Pharmaceutical compositions comprising antibodies for treatment of c1s mediated disorders and methods of using the same

Abstract

Provided for herein are pharmaceutical compositions comprising a therapeutic antibody and uses thereof for the treatment of C1s mediated disorders.

Description

PHARMACEUTICAL COMPOSITIONS COMPRISING ANTIBODIES FOR TREATMENT OF CIS MEDIATED DISORDERS AND METHODS OF USING THE SAMECROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application is a continuation-in-part of, and claims priority to, International Application No. PCT / CN2023 / 140449, filed December 20, 2023, and this application claims priority to Chinese Application No. 202411844428.4, filed December 13, 2024, each of which is hereby incorporated by reference in its entirety.REFERENCE TO SEQUENCE LISTING SUBMITTED ELECTRONICALLY

[0002] The instant application contains a Sequence Listing which has been submitted electronically in XML file format and is hereby incorporated by reference in its entirety. Said XML copy, created on October 31, 2024, is named “DIN-003 WO2 Sequence listings. xml” and is 494,661 bytes in size.FIELD

[0003] Embodiments provided herein related to therapeutic antibodies, and pharmaceutical compositions comprising the same for the treatment of Cis mediated disorders.BACKGROUND

[0004] The complement system is a well-known effector mechanism of the innate immune response, providing not only protection against pathogens and other harmful agents but also recovery from injury. Complement activation due to autoantibodies and alloantibodies can lead to damage to normal cells or rejection of transplanted tissue. The complement pathway comprises a number of proteins that typically exist in the body in inactive form. The classical complement pathway is triggered by activation of the first component of complement, referred to as the Cl complex, which consists of Clq, Clr, and Cis proteins. Upon binding of Cl to an immune complex or other activator, the Cis component, a diisopropyl fluorophosphate (DFP)-sensitive serine protease, cleaves complement components C4 and C2 to initiate activation of the classical complement pathway. The classical complement pathway appears to play a role in many diseases and disorders. For example, sutimlimab (TNT009), marketed as EnJaymo®, is an antibody that inhibits Cis for treatment of hemolysis in adults with cold agglutinin disease. However, sutimlimab binds to both the active form of Cis, and the inactive zymogen proCis, and due to the lack ofspecificity of sutimlimab for either form of Ci s, a very high dose must be administered to overcome circulating levels of proCis, and may limit the clinical use of sutimlimab. Therefore, there is a need in the art for compounds that treat a complement classical pathway-mediated disease or disorder with specificity for active forms of the complement proteins and pharmaceutically acceptable formulations to safely and effectively store and administer these compounds in a therapeutic setting. The embodiments provided for herein satisfy these needs as well as others.SUMMARY

[0005] Disclosed herein are pharmaceutical compositions for treating Cis mediated disorders and dosage forms, kits, and administration methods thereof. Embodiments disclosed herein are incorporated by reference into this section.

[0006] In some embodiments, an antibody, or antigen binding fragment thereof, is provided that binds to the active form of Cis. In some embodiments, an antibody, or antigen binding fragment thereof, is provided that specifically binds to the active form of Cis. In some embodiments, the antibody, or antigen binding fragment thereof, is as provided herein.DETAILED DESCRIPTION

[0007] Provided herein are binding proteins, e.g., antibodies, or fragments thereof, that selectively bind to Cis and have low binding to the zymogen proCis. In some embodiments, the antibodies inhibit activation of the classical complement pathway and can be used in methods to treat complement mediated disorders, such as, but not limited to those provided for herein. In some embodiments, the selectivity for Cis over proCis can be used to reduce or prevent target mediated clearance of the therapeutic antibody, thus requiring lower doses and frequency of administration of the antibody.

[0008] Also provided herein are pharmaceutical compositions of antibodies that bind and modulate the activity of Cis. The antibodies can be used, for example, to treat Cis mediated disorders.

[0009] It is to be understood that the embodiments described herein are not limited to particular formulations, compositions and experimental conditions disclosed, as such formulations, compositions, and experimental conditions may vary. It is also to be understood that the terminology used herein is only for the purpose of describing particular embodiments, and it is not intended to be limiting.

[0010] The following explanations of terms and methods are provided to better describe the present disclosure and to guide those of ordinary skill in the art in the practice of the present disclosure.

[0011] Those of ordinary skill in the art will understand that given the amino acid sequence of a variable region of the binding molecules (e.g., antibodies) set forth herein can determine the complementarity determining region (CDR) sequences therein by these or any other conventions used to define CDR, such as, for example, IMGT, Kabat, Chothia, or Contact using web-based tools are available for determining the CDRs in such variable regions based on any known convention. Such tools include those found at www.abysis.org / abysi s / sequence_input / key_annotation / key_annotation. cgi and at www.novoprolabs.com / tools / cdr. Accordingly, the disclosure herein of a set of three CDRs in a heavy or light chain variable region based upon one CDR convention is considered the equivalent of that same set of CDRs as determined by any other convention, which can be referred to as “convention equivalents” or “convention equivalent CDRs”.

[0012] Furthermore, the formulations, compositions, and experimental conditions described herein, unless otherwise indicated, use conventional molecular and cellular biological and immunological techniques known within the skill of the art. Such techniques are well known to the skilled worker, and are explained fully in the literature, (see, e.g., Ausubel, et al., ed., Current Protocols in Molecular Biology, John Wiley & Sons, Inc., NY, N.Y. (1987-2008), including all supplements, Molecular Cloning: A Laboratory Manual (Fourth Edition), by MR Green and J. Sambrook and Harlow et al., Antibodies: A Laboratory Manual, Chapter 14, Cold Spring Harbor Laboratory, Cold Spring Harbor (2013, 2ndedition)).

[0013] Unless otherwise defined, scientific and technical terms used herein have the meanings that are commonly understood by those of ordinary skill in the art. In the event of any latent ambiguity, definitions provided herein take precedent over any dictionary or extrinsic definition.

[0014] Unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular.

[0015] The use of “or” means “and / or” unless stated otherwise. The use of the term “including,” as well as other forms, such as “includes” and “included,” is not limiting.

[0016] Generally, nomenclature used in connection with cell and tissue culture, molecular biology, immunology, microbiology, genetics, and protein and nucleic acid chemistry and hybridization describedherein is well-known and commonly used in the art. The methods and techniques provided herein are generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present specification unless otherwise indicated. Enzymatic reactions are performed according to manufacturer’s specifications, as commonly accomplished in the art or as described herein. The nomenclatures used in connection with the laboratory procedures and techniques of analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those well-known and commonly used in the art.

[0017] As used herein, the terms “a” or “and” means that “at least one” or “one or more” unless the context clearly indicates otherwise.

[0018] As used herein, the term “about” means that the numerical value is approximate and small variations would not significantly affect the practice of the disclosed embodiments. Where a numerical limitation is used, unless indicated otherwise by the context, “about” means the numerical value can vary by ±10% and remain within the scope of the disclosed embodiments. Additionally, where a phrase recites “about x to y”, the term “about” modifies both x and y and can be used interchangeably with the phrase “about x to about y” unless context dictates differently.

[0019] As used herein, the terms “comprising” (and any form of comprising, such as “comprise”, “comprises” and “comprised”), “having” (and any form of having, such as “have” and “has”), “including” (and any form of including, such as “includes” and “include”), or “containing” (and any form of containing, such as “contains” and “contain”), are inclusive or open-ended and do not exclude additional, unrecited elements or method steps. Any step or composition that uses the transitional phrase of “comprise” or “comprising” can also be said to describe the same with the transitional phase of “consisting of’ or “consists of’. Further, the singular forms “a” or “an” or “the” include plural references unless the context clearly dictates otherwise. For example, reference to “comprising a therapeutic agent” includes one or a plurality of such therapeutic agents. The term “or” refers to a single element of stated alternative elements, unless the context clearly indicates otherwise. For example, the phrase “A or B” refers to A alone or B alone. The phrase “A, B, or a combination thereof’ refers to A alone, B alone, or a combination of A and B. Similarly, “one or more of A and B” refers to A, B, or a combination of both A and B. The phrase “A and B” refers to a combination of A and B. Furthermore, the various elements, features andsteps discussed herein, as well as other known equivalents for each such element, feature or step, can be mixed and matched by one of ordinary skill in this art to perform methods in accordance with principles described herein. Among the various elements, features, and steps some will be specifically included and others specifically excluded in particular examples.

[0020] A “disease” in an animal is a state of health wherein the animal cannot maintain homeostasis, and wherein if the disease is not ameliorated then the animal’s health continues to deteriorate. In contrast, a “disorder” in an animal is a state of health in which the animal is able to maintain homeostasis, but in which the animal’s state of health is less favorable than it would be in the absence of the disorder. Left untreated, a disorder does not necessarily cause a further decrease in the animal’s state of health.

[0021] ‘ ‘Parenteral” administration of a composition includes, e g., subcutaneous (s.c.), intravenous (i.v ), intramuscular (i.m ), or intracisternal injection, intrathecal, or infusion techniques.

[0022] The term “therapeutic” as used herein means a treatment and / or prophylaxis. A therapeutic effect is obtained by suppression, remission, or eradication of a disease state.

[0023] Throughout this disclosure, various aspects of the embodiments can be presented in a range format. It should be understood that the description in the range format is merely for convenience and brevity and should not be construed as an inflexible limitation. Accordingly, the description of a range should be considered to have specifically disclosed all the possible subranges as well as individual numerical values within that range. For example, description of a range such as from 1 to 6 should be considered to have specifically disclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from 2 to 4, from 2 to 6, from 3 to 6, etc., as well as the individual numbers within that range, for example, 1, 2, 2.7, 3, 4, 5, and 6. This applies regardless of the breadth of the range. Unless otherwise explicitly stated to the contrary, a range that is disclosed also includes the endpoints of the range.

[0024] The term “composition” as used herein means a product which results from the mixing or combining of more than one element or ingredient.

[0025] As used herein, the term “pharmaceutical composition” refers to a medicinal or pharmaceutical formulation that contains an active ingredient as well as one or more excipients and diluents to enable the active ingredient suitable for the method of administration.

[0026] The term “carrier” as used herein encompasses carriers, excipients, and diluents, meaning a material, composition or vehicle, such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material involved in carrying or transporting a pharmaceutical, cosmetic or other agent across a tissue layer.

[0027] The phrase “pharmaceutically acceptable” is employed herein to refer to those agents of interest, compounds, salts, compositions, pharmaceutical dosage forms, etc., which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and / or other mammals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit / risk ratio. In some embodiments, pharmaceutical acceptable means approved by a regulatory agency of the federal or a state government, or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for the use in animals (e g., mammals), and more particularly, in humans.

[0028] As used herein, the term “pharmaceutically acceptable carrier” refers to an excipient or diluent in a pharmaceutical composition. The pharmaceutically acceptable carrier must be compatible with the other ingredients of the formulation and not deleterious to the recipient. The nature of the carrier differs with the mode of administration. For example, for intravenous administration, an aqueous solution carrier is generally used; for oral administration, a solid carrier is generally used.

[0029] As used herein, “stable” a “stable composition” or a “stable pharmaceutical composition” refers to a composition or pharmaceutical composition that maintains one or more of the characteristics of the composition within a defined margin when subject to various stressors such as, but not limited to, heat, agitation, light, temperature, humidity, repeated freeze thaw cycles, and extended storage. Such characteristics include, but are not limited to, pH, presence of aggregates, functional titer, or concentration of protein excipient. In some embodiments, the defined margins for pH, presence of aggregates, functional titer, or concentration of protein excipient are as provided for herein.

[0030] As used herein, the term “antibody” refers to any form of antibody that exhibits the desired biological activity. Thus, it is used in the broadest sense and specifically covers, but is not limited to, monoclonal antibodies (including full length monoclonal antibodies), polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), humanized, fully human antibodies, chimeric antibodies and camelized single domain antibodies. An antibody consists of four polypeptide chains; two heavy chains(CHI and Cu2) and two light chains (CLI and CL2) connected by disulfide bonds. Each chain is a series of domains: light chains consist of one variable domain (VL) and one constant domain (CL), while heavy chains contain one variable domain (VH) and three to four constant domains (CHI, CH2, CH3, CH4). “Parental antibodies” are antibodies obtained by exposure of an immune system to an antigen prior to modification of the antibodies for an intended use, such as humanization of an antibody for use as a human therapeutic antibody.

[0031] As used herein, unless otherwise indicated, “antibody fragment” or “antigen binding fragment” refers to antigen binding fragments of antibodies, i.e., antibody fragments that retain the ability to bind specifically to the antigen bound by the full-length antibody, e.g., fragments that retain one or more CDR regions. Examples of antibody binding fragments include, but are not limited to, Fab, Fab', F(ab')2, Fv fragments, diabodies, linear antibodies, single-chain antibody molecules, e g., sc-Fv, nanobodies and multispecific antibodies formed from antibody fragments.

[0032] A “Fab fragment” is comprised of one light chain and the Cui and variable regions of one heavy chain. The heavy chain of a Fab molecule cannot form a disulfide bond with another heavy chain molecule.

[0033] An “Fc” region contains two heavy chain fragments comprising the CH2 and CH3 domains of an antibody. The two heavy chain fragments are held together by two or more disulfide bonds, and by hydrophobic interactions of the CH3 domains.

[0034] As used herein, the term “fused” or “linked” when used in reference to a protein having different domains or heterologous sequences means that the protein domains are part of the same peptide chain that are connected to one another with either peptide bonds or other covalent bonding. The domains or section can be linked or fused directly to one another or another domain or peptide sequence can be between the two domains or sequences and such sequences would still be considered to be fused or linked to one another. In some embodiments, the various domains or proteins provided for herein are linked or fused directly to one another or a linker sequences, such as a glycine / serine, glycine / alanine linker, or other types of peptide linkers generally known to link the two domains together. Two peptide sequences are linked directly if they are directly connected to one another, or indirectly if there is a linker or other structure that links the two regions. A linker can be directly linked to two different peptide sequences or domains.

[0035] A “Fab1fragment” contains one light chain and a portion or fragment of one heavy chain that contains the VH domain and the CHI domain and also the region between the CHI and CH2 domains, such that an interchain disulfide bond can be formed between the two heavy chains of two Fab' fragments to form a F(ab') 2 molecule.

[0036] A “F(ab')2 fragment” contains two light chains and two heavy chains containing a portion of the constant region between the CHI and CH2 domains, such that an interchain disulfide bond is formed between the two heavy chains. A F(ab') 2 fragment thus is composed of two Fab' fragments that are held together by a disulfide bond between the two heavy chains.

[0037] The “Fv region” comprises the variable regions from both the heavy and light chains, but lacks the constant regions.

[0038] The term “single-chain Fv” or “scFv” antibody refers to antibody fragments comprising the VH and VL domains of an antibody, wherein these domains are present in a single polypeptide chain. Generally, the Fv polypeptide further comprises a polypeptide linker between the VH and VL domains which enables the scFv to form the desired structure for antigen binding. For a review of scFv, see Pluckthun (1994) THE PHARMACOLOGY OF MONOCLONAL ANTIBODIES, vol. 113, Rosenburg and Moore eds. Springer-Verlag, New York, pp. 269-315; International Patent Application Publication No. WO 88 / 01649; and U.S. Pat. Nos. 4,946, 778 and 5,260,203.

[0039] A “domain antibody” is an immunologically functional immunoglobulin fragment containing only the variable region of a heavy chain or the variable region of a light chain. In some instances, two or more VH regions are covalently j oined with a peptide linker to create a bivalent domain antibody. The two VH regions of a bivalent domain antibody may target the same or different antigens.

[0040] A “bivalent antibody” comprises two antigen binding sites. In some instances, the two binding sites have the same antigen specificities. However, bivalent antibodies may be bispecific (see below).

[0041] A “single-domain antibody” is an immunologically functional immunoglobulin fragment containing only the variable region of a heavy chain or the variable region of a light chain. In some instances, two or more VH regions are covalently joined with a peptide linker to create a bivalent domain antibody.

[0042] In some embodiments, as provided for herein, antibody molecules can be monospecific (e.g., monovalent or bivalent), bispecific (e.g., bivalent, trivalent, tetravalent, pentavalent, or hexavalent), trispecific (e.g., trivalent, tetravalent, pentavalent, hexavalent), or with higher orders of specificity (e.g., tetraspecific) and / or higher orders of valency beyond hexavalency. An antibody molecule can comprise a functional fragment of a light chain variable region and a functional fragment of a heavy chain variable region, or heavy and light chains may be fused together into a single polypeptide.

[0043] In some embodiments, monoclonal antibodies herein also include camelized single domain antibodies (see, e.g., Muyldermans et al. (2001) Trends Biochem. Sci. 26:230; Reichmann et al. (1999) J. Immunol. Methods 231 :25; WO 94 / 04678; WO 94 / 25591; U.S. Pat. No. 6,005,079)). In some embodiments, the present disclosure provides single domain antibodies comprising two VH domains with modifications such that single domain antibodies are formed.

[0044] As used herein, the term “diabodies” refers to small antibody fragments with two antigen-binding sites, which fragments comprise a heavy chain variable domain (VH) connected to a light chain variable domain (VL) in the same polypeptide chain (VH-VL or VL-VH). By using a linker that is too short to allow pairing between the two domains on the same chain, the domains are forced to pair with the complementary domains of another chain and create two antigen-binding sites. Diabodies are described more fully in, e.g., EP 404,097; WO 93 / 11161; and Holliger et al. (1993) Proc. Natl. Acad. Sci. USA 90: 6444-6448. For a review of engineered antibody variants generally see Holliger and Hudson (2005) Nat. Biotechnol. 23:1126-1136.

[0045] Typically, a variant antibody or antigen binding fragment of the antibodies provided herein retain at least 10% of its Cis binding activity (when compared to a parental antibody that is modified) when that activity is expressed on a molar basis. In some embodiments, a variant antibody, or antigen fragment thereof, or antigen binding fragment of an antibody provided herein, retains at least 20%, 50%, 70%, 80%, 90%, 95% or 100% or more of the Cis binding affinity as the parental antibody. As described herein, it is also intended that an antibody or antigen binding fragment of the disclosure can include conservative or non-conservative amino acid substitutions, which can also be referred to as “conservative variants” or “function conserved variants” of the antibody, that do not substantially alter its biologic activity.

[0046] “Isolated antibody” refers to the purification status of a binding compound and in such context means the molecule is substantially free of other biological molecules such as nucleic acids, proteins,lipids, carbohydrates, or other material such as cellular debris and growth media. Generally, the term “isolated” is not intended to refer to a complete absence of such material or to an absence of water, buffers, or salts, unless they are present in amounts that substantially interfere with experimental or therapeutic use of the binding compound as described herein.

[0047] The term “monoclonal antibody”, as used herein, refers to population of substantially homogeneous antibodies, i.e., the antibody molecules comprising the population are identical in amino acid sequence except for possible naturally occurring mutations and / or post-translational modifications that may be present in minor amounts. In contrast, conventional (polyclonal) antibody preparations typically include a multitude of different antibodies having different amino acid sequences in their variable domains, particularly their CDRs, that are often specific for different epitopes. The modifier “monoclonal” indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method. For example, the monoclonal antibodies to be used in accordance with the present invention may be made by the hybridoma method first described by Kohler et al. (1975) Nature 256: 495, or may be made by recombinant DNA methods (see, e.g., U.S. Pat. No. 4,816,567). The “monoclonal antibodies” may also be isolated from phage antibody libraries using the techniques described in Clackson et al. (1991) Nature 352: 624-628 and Marks et al. (1991) J. Mol. Biol. 222: 581-597, for example. See also Presta (2005) J. Allergy Clin. Immunol. 116:731.

[0048] As used herein, a “chimeric antibody” is an antibody having the variable domain from a first antibody and constant domain from a second antibody, where the first and second antibodies are from different species. (U.S. Pat. No. 4,816,567; and Morrison et al., (1984) Proc. Natl. Acad. Sci. USA 81 : 6851-6855). Typically, the variable domains are obtained from an antibody from an experimental animal (the “parental antibody”), such as a rodent, and the constant domain sequences are obtained from human antibodies, so that the resulting chimeric antibody will be less likely to elicit an adverse immune response in a human subject than the parental (e.g. rodent) antibody.

[0049] As used herein, the term “humanized antibody” refers to forms of antibodies that contain sequences from both human and non-human (e.g., murine, rat) antibodies. In general, the humanized antibody will comprise substantially all of at least one, and typically two, variable domains, in which all or substantially all of the hypervariable loops correspond to those of a non-human immunoglobulin, and all or substantiallyall of the framework (FR) regions are those of a human immunoglobulin sequence. The humanized antibody may optionally comprise at least a portion of a human immunoglobulin constant region (Fc).

[0050] The term “fully human antibody” refers to an antibody that comprises human immunoglobulin protein sequences only. A fully human antibody may contain murine carbohydrate chains if produced in a mouse, a mouse cell, or a hybridoma derived from a mouse cell. Similarly, “mouse antibody” refers to an antibody that comprises mouse immunoglobulin sequences only. Alternatively, a fully human antibody may contain rat carbohydrate chains if produced in a rat, a rat cell, or a hybridoma derived from a rat cell. Similarly, “rat antibody” refers to an antibody that comprises rat immunoglobulin sequences only.

[0051] In some embodiments, the basic antibody structural unit comprises a tetramer. Each tetramer includes two identical pairs of polypeptide chains, each pair having one “light” (about 25 kDa) and one “heavy” chain (about 50-70 kDa). The amino-terminal portion of each chain includes a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The carboxy -terminal portion of the heavy chain may define a constant region primarily responsible for effector function. Typically, human light chains are classified as kappa and lambda light chains. Furthermore, human heavy chains are typically classified as mu, delta, gamma, alpha, or epsilon, and define the antibody's isotype as IgM, IgD, IgG, IgA, and IgE, respectively. Within light and heavy chains, the variable and constant regions are joined by a “J” region of about 12 or more amino acids, with the heavy chain also including a “D” region of about 10 more amino acids. See generally, Fundamental Immunology Ch. 7 (Paul, W , ed., 2nd ed. Raven Press, N.Y. (1989).

[0052] The variable regions of each light / heavy chain pair form the antibody binding site. Thus, in general, an intact antibody has two binding sites. However, in bifunctional or bispecific antibodies, the two binding sites are, in general, not the same.

[0053] Typically, the variable domains of both the heavy and light chains comprise three hypervariable regions, also called complementarity determining regions (CDRs), located within relatively conserved framework regions (FR). The CDRs are usually aligned by the framework regions, enabling binding to a specific epitope. In general, from N-terminal to C-terminal, both light and heavy chains variable domains comprise FR1, CDR1, FR2, CDR2, FR3, CDR3 and FR4. The assignment of amino acids to each domain is, generally, in accordance with the definitions of Sequences of Proteins of Immunological Interest, Kabat, et al:, National Institutes of Health, Bethesda, Md.; 5thed.; NIH Publ. No. 91-3242 (1991); Kabat(1978) Adv. Prot. Chem. 32:1 -75; Kabat, et al., (1977) J. Biol. Chem. 252:6609-6616; Chothia, et al., (1987) J Mol. Biol. 196:901-917 or Chothia, etal., (1989) Nature 342:878-883.

[0054] As used herein, the term “hypervariable region” refers to the amino acid residues of an antibody that are responsible for antigen-binding. The hypervariable region comprises amino acid residues from a “complementarity determining region” or “CDR” (i.e. residues 24-34 (CDRL1), 50-56 (CDRL2) and 89- 97 (CDRL3) in the light chain variable domain and residues 31-35 (CDRH1), 50-65 (CDRH2) and 95- 102 (CDRH3) in the heavy chain variable domain; Kabat el al. (1991) Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md.) and / or those residues from a “hypervariable loop” (i.e. residues 26-32 (CDRL1), 50-52 (CDRL2) and 91- 96 (CDRL3) in the light chain variable domain and 26-32 (CDRH1), 53-55 (CDRH2) and 96-101 (CDRH3) in the heavy chain variable domain (Chothia and Lesk (1987) J. Mol. Biol. 196: 901-917)). The CDRs can also be referenced according to the IMGT system for the identification of CDRs, which is described in Lefranc MP. Unique database numbering system for immunogenetic analysis. (Immunol Today (1997) 18:509).

[0055] As used herein, the term “framework” or “FR” residues refers to those variable domain residues other than the hypervariable region residues defined herein as CDR residues. CDRs provide the majority of contact residues for the binding of the antibody to the antigen or epitope. CDRs of interest can be derived from donor antibody variable heavy and light chain sequences, and include analogs of the naturally occurring CDRs, which analogs also share or retain the same antigen binding specificity and / or neutralizing ability as the donor antibody from which they were derived.

[0056] As used herein, “specific binding” or “immunospecific binding” or “binds immunospecifically” refer to antibody binding to a predetermined antigen at a much higher affinity than for another antigen(s) (e.g. selectively binds the active form of complement component Cis as compared to inactive Cis, which can also be referred to as proCis zymogen). In some embodiments, the antibody binds the predetermined antigen with a dissociation constant (KD) of 10’7M or less, and such Ko is at least two-fold less than its KD for binding to a non-specific antigen (e.g., BSA, casein, or another non-specific polypeptide).

[0057] The phrases “an antibody recognizing Cis” and “an antibody specific for Cis” are used interchangeably herein with the term “an antibody which binds immunospecifically to Cis”. In some embodiments, the antibody binds specifically or preferentially to Cis, such as the active form of Cis overother proteins, such as, but not limited to, the inactive form of Ci s (proCi s). The degree of specificity necessary for an anti-Cls antibody may depend on the intended use of the antibody, and at any rate is defined by its suitability for use for an intended purpose. In some embodiments, the antibody, or binding compound derived from the antigen-binding site of an antibody, of the contemplated method binds to its antigen (active form of Cis), with an affinity that is at least two-fold greater, at least ten times greater, at least 20-times greater, or at least 100-times greater than the affinity with any other antigen, including, but not limited to inactive Cis.

[0058] Methods for determining mAb specificity and affinity by competitive inhibition can be found in Harlow, et al., Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1988), Colligan et al., eds., Current Protocols in Immunology, Greene Publishing Assoc, and Wiley Interscience, N.Y., (1992, 1993), and Muller, Meth. Enzymol. 92:589 601 (1983), which references are entirely incorporated herein by reference.

[0059] The term “homolog” means protein sequences having between 40% and 100% sequence identity to a reference sequence. Percent identity between two peptide chains can be determined by pair wise alignment using the default settings of the AlignX module of Vector NTI v.9.0.0 (Invitrogen Corp., Carlsbad, Calif.) or other suitable alignment software, such as BLAST. In some embodiments, the antibody, or antigen binding fragment thereof has, at least 50, 60, 70, 80, 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99% homology or identity to a sequence described herein. In some embodiments, the antibody has conservative substitutions as compared to a sequence described herein. Exemplary conservative substitutions are illustrated in Table 1 and are encompassed within the scope of the disclosed subject matter. The conservative substitution may reside in the framework regions, or in antigen-binding sites, as long they do not adversely affect the properties of the antibody. Substitutions may be made to improve antibody properties, for example stability or affinity. Conservative substitutions will produce molecules having functional and chemical characteristics similar to those molecules into which such modifications are made. Exemplary amino acid substitutions are shown in the table below.

[0060] Table 1: Exemplary Conservative Substitutions

[0061] In some embodiments, variants of the proteins and peptides provided herein are provided. In some embodiments, a variant comprises a substitution, deletions, or insertion. In some embodiments, the variant comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 (e.g., 1-10) substitutions. As described herein, the substitutions can be conservative substitutions. In some embodiments, the substitution is non-conservative. In some embodiments, the variant comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 (e.g., 1-10) deletions. In some embodiments, the variant comprises 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 (e.g., 1-10) insertions. In some embodiments, the substitutions, deletions, or insertions are present in the CDRs provided for herein. In some embodiments, the substitutions, deletions, or insertions are not present in the CDRs provided for herein.

[0062] The term “in combination with” as used herein means that the described agents can be administered to an animal or subject together in a mixture, concurrently as single agents or sequentially as single agents in any order.

[0063] The term “epitope” is meant to refer to that portion of any molecule capable of being recognized by and bound by an antibody at one or more of the Ab’s antigen binding regions. Epitopes usually consist of chemically active surface groupings of molecules such as amino acids or sugar side chains and have specific three-dimensional structural characteristics as well as specific charge characteristics.

[0064] “Expression vector” refers to a vector comprising a recombinant polynucleotide comprising expression control sequences operatively linked to a nucleotide sequence to be expressed. An expression vector comprises sufficient cis-acting elements for expression; other elements for expression can be supplied by the host cell or in an / / / vitro expression system. Expression vectors include all those known in the art, such as cosmids, plasmids (e.g., naked or contained in liposomes) and viruses (e.g., Sendai viruses, lentiviruses, retroviruses, adenoviruses, and adeno-associated viruses) that incorporate the recombinant polynucleotide.

[0065] In some embodiments, the antibody is a monoclonal antibody which binds to Cis. The sequence of active Cis is as follows (SEQ ID NO: 258), and residues 1-15 (SEQ ID NO: 259) constitute the signal peptide which is cleaved during translation, while residues 16-688 (SEQ ID NO: 260) constitute the mature protein:MWCIVLFSLLAWVYAEPTMYGEILSPNYPQAYPSEVEKSWDIEVPEGYGIHLYFTHLDI ELSENC AYDSVQIISGDTEEGRLCGQRS SNNPHSPIVEEFQ VP YNKLQVIFK SDF SNEER FTGFAAYYVATDINECTDFVDVPCSHFCNNFIGGYFCSCPPEYFLHDDMKNCGVNCSG DVFTALIGEIASPNYPKPYPENSRCEYQIRLEKGFQVVVTLRREDFDVEAADSAGNCLD SLVFVAGDRQFGPYCGHGFPGPLNIETKSNALDIIFQTDLTGQKKGWKLRYHGDPMPC PKEDTPNSVWEPAKAKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGKWSNSK LKCQPVDCGIPESIENGKVEDPESTLFGSVIRYTCEEPYYYMENGGGGEYHCAGNGSW VNEVLGPELPKCVPVCGVPREPFEEKQRIIGGSDADIKNFPWQVFFDNPWAGGALINE YWVLTAAHVVEGNREPTMYVGSTSVQTSRLAKSKMLTPEHVFIHPGWKLLEVPEGRT NFDNDIALVRLKDPVKMGPTVSPICLPGTSSDYNLMDGDLGLISGWGRTEKRDRAVRL KAARLPVAPLRKCKEVKVEKPTADAEAYVFTPNMICAGGEKGMDSCKGDSGGAFAV QDPNDKTKFYAAGLVSWGPQCGTYGLYTRVKNYVDWIMKTMQENSTPRED (SEQ ID NO: 258);MWCIVLFSLLAWVYA (SEQ ID NO: 259);EPTMYGEILSPNYPQAYPSEVEKSWDIEVPEGYGIHLYFTHLDIELSENCAYDSVQIISG DTEEGRLCGQRS SNNPHSPIVEEFQ VP YNKLQ VIFKSDF SNEERFTGF AAYYVATDINE CTDFVDVPCSHFCNNFIGGYFCSCPPEYFLHDDMKNCGVNCSGDVFTALIGEIASPNYP KPYPENSRCEYQIRLEKGFQVVVTLRREDFDVEAADSAGNCLDSLVFVAGDRQFGPYCGHGFPGPLNIETKSNALDIIFQTDLTGQKKGWKLRYHGDPMPCPKEDTPNSVWEPAK AKYVFRDVVQITCLDGFEVVEGRVGATSFYSTCQSNGKWSNSKLKCQPVDCGIPESIE NGKVEDPESTLFGSVIRYTCEEPYYYMENGGGGEYHCAGNGSWVNEVLGPELPKCVP VCGVPREPFEEKQRIIGGSDADIKNFPWQVFFDNPWAGGALINEYWVLTAAHVVEGN REPTMYVGSTSVQTSRLAKSKMLTPEHVFIHPGWKLLEVPEGRTNFDNDIALVRLKDP VKMGPTVSPICLPGTSSDYNLMDGDLGLISGWGRTEKRDRAVRLKAARLPVAPLRKC KEVKVEKPTADAEAYVFTPNMICAGGEKGMDSCKGDSGGAFAVQDPNDKTKFYAAG LVSWGPQCGTYGLYTRVKNYVDWIMKTMQENSTPRED (SEQ ID NO: 260).

[0066] The difference between inactive Cis and active C 1 s is that inactive proC Is is cleaved at the peptide bond between R437 and 1438 and undergoes a conformational change. The two fragments generated by this cleavage remain associated by a disulfide bond. Without wishing to be bound by a particular theory, proCis is a single chain 86,000 Da protein that is the native form of Cis proteins (e.g., serine protease). Cis is a subunit of the Cl complex which is the first complement component in the cascade referred to as the classical pathway of complement. ProC Is is an inactive zymogen until Cl is activated. Cl complex binds to and is activated by antigen-antibody complexes (immune complexes) yielding Clr enzyme. Clr enzyme in the Cl complex activates proC Is generating Cis enzyme. Cl complex is a non-covalent calcium-dependent complex of one Clq, two Clr and two Cis molecules. Clq binds through two or more of its six arms to the Fc domains of IgG or IgM. The binding of multiple arms to immune complexes causes the two Clr proteins in the complex (protease zymogens) to activate producing two proteases that cleave and activate the two proC Is in the complex (Morikis, D. and Lambris, J.D. (2005)). This activation of proCis is caused by cleavage into the two chain Cis enzyme with 58,000 and 28,000 Dalton fragments.

[0067] In some embodiments, antibodies (e.g. an anti-Cls antibody) are provided herein. In some embodiments, the antibody is a recombinant antibody that binds to Cis. In some embodiments, the antibody binds to the active form of Cis. In some embodiments, the antibody binds to active form preferentially over the inactive form of Cis. In some embodiments, the antibody binds to the active form with an affinity that is at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, or 200% higher as compared to its affinity for the inactive form of Cis. In some embodiments, the Cis protein is a human Cis protein, such as the active form of Cis. In some embodiments, the antibody does not specifically bind to the inactive form of the Cis protein. As used herein, the term “recombinant antibody” refers to an antibody that is not naturally occurring. In some embodiments, the term “recombinant antibody” refers to an antibody that isnot isolated from a human subject. In some embodiments, the antibody binds with at least 100X more affinity to the active form of Cis as compared to proCis.

[0068] In some embodiments, an antibody, or antigen binding fragment thereof is provided, wherein the antibody or antibody fragment comprises a peptide selected from the following table, which illustrate the CDRs based on Kabat numbering.

[0069] The CDRs in the above-identified table can also be referred to according to Chothia CDRs or IMGT CDRs. These are illustrated in the following tables for the different antibodies.

[0070] In some embodiments, the antibody comprises a heavy chain variable region polypeptide having one of the sequences selected from the table below, or a variant thereof.

[0071] In some embodiments, the antibody comprises a light chain variable region polypeptide having one of the sequences selected from the table below, or a variant thereof.

[0072] In some embodiments, the antibody comprises a heavy chain as set forth in the table below, wherein the heavy chain comprises a heavy chain variable region and a constant domain.

[0073] In some embodiments, the antibody comprises a light chain as set forth in the table below, wherein the light chain comprises a light chain variable region and a constant domain, such as the human kappa constant domain.

[0074] In some embodiments, the antibody comprises an Fc domain. The Fc domain can be linked to the heavy or light chain of the antibody. In some embodiments, the Fc domain comprises a mutation to extend the half-life of the antibody. In some embodiments, the Fc domain comprises a mutation such as those described in U.S. Patent No. 7,670,600, which is hereby incorporated by reference in its entirety. In some embodiment, the constant region comprises a mutation at position at amino acid residue 428 relative to awild-type human IgG constant domain, numbered according to the EU numbering index of Kabat. Without being bound to any particular theory, an antibody comprising a mutation that corresponds to residue 428 can have an increased half-life compared to the half-life of an IgG having the wild-type human IgG constant domain. In some embodiments, the mutation is a substitution of the native residue with a threonine, leucine, phenylalanine or serine. In some embodiments, the antibody further comprises one or more amino acid substitutions relative to the corresponding wild-type human IgG constant domain at one or more of amino acid residues 251-256, 285-290, 308-314, 385-389, and 429-436, numbered according to the Kabat EU numbering index. The specific mutations or substitutions at these positions are described in U.S. Patent No. 7,670,600, which is hereby incorporated by reference in its entirety.

[0075] Other mutations can be used in the Fc domain, such as those provided for in U.S. Patent No. 8,394,925, which is hereby incorporated by reference in its entirety. In some embodiments, the Fc region is a variant Fc region comprising amino acid substitutions at positions 428 and 434, wherein the amino acid substitutions are a leucine that is not the wild-type amino acid at position 428 and a serine that is not the wild-type amino acid at position 434, wherein the polypeptide is an antibody and wherein numbering is according to the EU Index in Kabat et al. In some embodiments, the Fc region comprises a S228P, L235E, M428L, or N434S substitution. In some embodiments, the Fc region comprises a M428L substitution. In some embodiments, the Fc region comprises a N434S substitution. In some embodiments, the Fc region comprises a M428L and a N434S substitution. In some embodiments, the Fc region comprises a M252Y, S254T, and / or T256E substitution.

[0076] In some embodiments, the antibody comprises a constant region as set forth below with or without the mutations provided for in the list below:ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSL SSVVTVPSSSLGTKTYTCNVDHKPSNTKVDKRVESKYGPPCPPCPAPEFEGGPSVFLFPPKPKDT LMISRTPEVTCVVVDVSQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQD WLNGKEYKCKVSNKGLPSSIEKTISKAKGQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSD IAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVLHEALHSHYTQK SLSLSLGK (IgG4 S228P L235E LS; SEQ ID NO: 261); orASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSL S S VVTVP S S SLGTKTYTCNVDHKPSNTKVDKRVESKYGPPCPPCP APEFEGGP S VFLFPPKPKDT LYITREPEVTCVVVDVSQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQD WLNGKEYKCKVSNKGLPSSIEKTISKAKGQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSD IAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVMHEALHNHYTQK SLSLSLGK (IgG4 S228P L235E YTE; SEQ ID NO: 262).

[0077] In some embodiments, the antibody comprises a constant region as provided herein, wherein the C-terminal lysine (K) amino acid has been deleted. In some embodiments, the antibody comprises a constant region as set follows:ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSL S S VVTVP S S SLGTKTYTCNVDHKPSNTKVDKRVESKYGPPCPPCP APEFEGGP S VFLFPPKPKDT LMISRTPEVTCVVVDVSQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQD WLNGKEYKCKVSNKGLPSSIEKTISKAKGQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSD IAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVLHEALHSHYTQK SLSLSLG (IgG4 S228P L235E LS-trunc; SEQ ID NO: 263); orASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSL SSVVTVPSSSLGTKTYTCNVDHKPSNTKVDKRVESKYGPPCPPCPAPEFEGGPSVFLFPPKPKDT LYITREPEVTCVVVDVSQEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTYRVVSVLTVLHQD WLNGKEYKCKVSNKGLPSSIEKTISKAKGQPREPQVYTLPPSQEEMTKNQVSLTCLVKGFYPSD IAVEWESNGQPENNYKTTPPVLDSDGSFFLYSRLTVDKSRWQEGNVFSCSVMHEALHNHYTQK SLSLSLG (IgG4 S228P L235E YTE-trunc; SEQ ID NO: 264).

[0078] In some embodiments, the antibody, or the light chain of the antibody, comprises a kappa constant region, such as the human constant domain, which can comprise a sequence of:RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKD STYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC (human kappa constant domain, SEQ ID NO: 265).

[0079] The term “purified” with referenced to an antibody refers to an antibody that is substantially free of other material that associates with the molecule in its natural environment. For instance, a purifiedprotein is substantially free of the cellular material or other proteins from the cell or tissue from which it is derived. The term refers to preparations where the isolated protein is sufficiently pure to be analyzed, or at least 70% to 80% (w / w) pure, at least 80%-90% (w / w) pure, 90-95% pure; and, at least 95%, 96%, 97%, 98%, 99%, or 100% (w / w) pure. In some embodiments, the antibody is purified.PHARMACEUTICAL COMPOSITIONS

[0080] In some embodiments, a pharmaceutical composition is provided. In some embodiments, the pharmaceutical composition comprises an antibody or antigen-binding fragment thereof as provided for herein.

[0081] In some embodiments, to prepare pharmaceutical or sterile compositions of the anti-Cls antibodies or other proteins provided herein, the antibody, or antigen binding fragment thereof, or other proteins provided herein are admixed with a pharmaceutically acceptable carrier or excipient, (see, e.g, Remington's Pharmaceutical Sciences and U. S. Pharmacopeia: National Formulary, Mack Publishing Company, Easton, PA (1984)).

[0082] Formulations of therapeutic or the antibodies provided herein may be prepared by mixing with acceptable carriers, excipients, or stabilizers in the form of, e.g., lyophilized powders, slurries, aqueous solutions or suspensions (see, e.g., Hardman, et al. (2001) Goodman and Gilman ’s The Pharmacological Basis of Therapeutics, McGraw-Hill, New York, NY; Gennaro (2000) Remington: The Science and Practice of Pharmacy, Lippincott, Williams, and Wilkins, New York, NY; Avis, et al. (eds.) (1993) Pharmaceutical Dosage Forms: Parenteral Medications, Marcel Dekker, NY; Lieberman, et al. (eds.) (1990) Pharmaceutical Dosage Forms: Tablets, Marcel Dekker, NY; Lieberman, et al. (eds.) (1990) Pharmaceutical Dosage Forms: Disperse Systems, Marcel Dekker, NY; Weiner and Kotkoskie (2000) Excipient Toxicity and Safety, Marcel Dekker, Inc., New York, NY). In some embodiments, the antibodies are diluted to an appropriate concentration in a sodium acetate solution pH 5-6, and NaCl or sucrose is added for tonicity. Additional agents, such as polysorbate 20 or polysorbate 80, may be added to enhance stability.

[0083] Toxicity and therapeutic efficacy of the antibody compositions, administered alone or in combination with another agent, can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., for determining the LD50 (the dose lethal to 50% of the population) and the ED50 (the dose therapeutically effective in 50% of the population). The dose ratio between toxic andtherapeutic effects is the therapeutic index (LD50 / ED50). In some embodiments, antibodies exhibiting high therapeutic indices are desirable. The data obtained from these cell culture assays and animal studies can be used in formulating a range of dosage for use in human. The dosage of such compounds lies preferably within a range of circulating concentrations that include the ED50 with little or no toxicity. The dosage may vary within this range depending upon the dosage form employed and the route of administration.

[0084] In some embodiments, a composition is administered to a subject in accordance with the Physicians' Desk Reference 2003 (Thomson Healthcare; 57th edition (November 1, 2002)).

[0085] In some embodiments, the mode of administration may vary. Suitable routes of administration include oral, rectal, transmucosal, intestinal, parenteral; intramuscular, subcutaneous, intradermal, intramedullary, intrathecal, direct intraventricular, intravenous, intraperitoneal, intranasal, intraocular, inhalation, insufflation, topical, cutaneous, transdermal, or intra-arterial. In some embodiments, the composition is an injectable pharmaceutical composition. In some embodiments, the composition is formulated for intravenous or subcutaneous injection. In some embodiments, the composition is formulated for intravenous injection. In some embodiments, the composition is formulated for subcutaneous injection.

[0086] In some embodiments, the antibody, or antigen binding fragment thereof, can be administered by an invasive route such as by injection. In some embodiments, the antibodies or antigen binding fragment thereof, or pharmaceutical composition thereof, is administered intravenously, subcutaneously, intramuscularly, intraarterially, intra-articularly (e.g. in arthritis joints), intratumorally, or by inhalation, such as through an aerosol delivery. Administration by non-invasive routes (e.g., orally; for example, in a pill, capsule or tablet) is also within the scope of the present embodiments.

[0087] In some embodiments, the anti -Cis antibody, or antigen binding fragment thereof, is administered in combination with at least one additional therapeutic agent, such as, but not limited to any therapeutic used to treat the disorders provided for herein. In some embodiments, the antibody is administered in combination with another treatment for the disorders provided for herein.

[0088] Compositions can be administered with medical devices known in the art. For example, a pharmaceutical composition of the invention can be administered by injection with a hypodermic needle, including, e.g., a prefilled syringe or an autoinjector.

[0089] The pharmaceutical compositions may also be administered with a needleless hypodermic injection device; such as the devices disclosed in U.S. Patent Nos. 6,620,135; 6,096,002; 5,399,163; 5,383,851; 5,312,335; 5,064,413; 4,941,880; 4,790,824 or 4,596,556.

[0090] The pharmaceutical compositions may also be administered by infusion. Examples of well-known implants and modules form administering pharmaceutical compositions include: U.S. Patent No. 4,487,603, which discloses an implantable micro-infusion pump for dispensing medication at a controlled rate; U.S. Patent No. 4,447,233, which discloses a medication infusion pump for delivering medication at a precise infusion rate; U.S. Patent No. 4,447,224, which discloses a variable flow implantable infusion apparatus for continuous drug delivery; U.S. Patent. No. 4,439,196, which discloses an osmotic drug delivery system having multi-chamber compartments. Many other such implants, delivery systems, and modules are well known to those skilled in the art.

[0091] Other devices that can also be used, including, but are not limited to those provided for in U.S. Patent No. 11779704, U.S. Patent No. 11654244, U.S. Patent No. 11612690, U.S. Patent No. 11607494, U.S. Patent No. 11602596, U.S. Patent No. 11541189, U.S. Patent No. 11534556, U.S. Patent No. 11524118, U.S. Patent No. 11458257, U.S. Patent No. 11458254, U.S. Patent No. 11426529, U.S. Patent No. 11426524, U.S. Patent No. 11406768, U.S. Patent No. 11383044, U.S. Patent No. 11331437, U.S. Patent No. 11311681, U.S. Patent No. 11291771, U.S. Patent No. 11273265, U.S. Patent No. 11253653, U.S. Patent No. 11229748, U.S. Patent No. 11224697, U.S. Patent No. 11154654, U.S. Patent No. 11141536, U.S. Patent No. 11103647, U.S. Patent No. 11103646, U.S. Patent No. 11065393, U.S. Patent No. 11058822, U.S. Patent No. 10983187, U.S. Patent No. 10980947, U.S. Patent No. 10973988, U.S. Patent No. 10960143, U.S. Patent No. 10894127, U.S. Patent No. 10881799, U.S. Patent No. 10850032, U.S. Patent No. 10814066, U.S. Patent No. 10799647, U.S. Patent No. 10709840, U.S. Patent No. 10632260, U.S. Patent No. 10610646, U.S. Patent No. 10603443, U.S. Patent No. 10596327, U.S. Patent No. 10569025, U.S. Patent No. 10569019, U.S. Patent No. 10561799, U.S. Patent No. 10537685, U.S. Patent No. 10518035, U.S. Patent No. 10493213, U.S. Patent No. 10493212, U.S. Patent No. 10485933, U.S. Patent No. 10471215, U.S. Patent No. 10441729, U.S. Patent No. 10413673, U.S. Patent No. 10376641, U.S. Patent No. 10350363, U.S. Patent No. 10350359, U.S. Patent No. 10350358, U.S. Patent No. 10350356, U.S. Patent No. 10335543, U.S. Patent No. 10331996, U.S. Patent No. 10300211, U.S. Patent No. 10201659, U.S. Patent No. 10149948, U.S. Patent No. 10149945, U.S. Patent No. 10143806, U.S. PatentNo. 10137253, U.S. PatentNo. 10099017, U.S. PatentNo. 9962496, U.S. PatentNo. 9962495,U.S. Patent No. 9867948, U.S. Patent No. 9855392, U.S. Patent No. 9821121, U.S. Patent No. 9750887,U.S. Patent No. 9744311, U.S. Patent No. 9566389, U.S. Patent No. 9539385, U.S. Patent No. 9457156,U.S. Patent No. 9320853, U.S. Patent No. 9289561, U.S. Patent No. 9278178, U.S. Patent No. 9205195,U.S. Patent No. 9138543, U.S. Patent No. 9057369, U.S. Patent No. 8998876, U.S. Patent No. 8992487,U.S. PatentNo. 8956330, U.S. Patent No. 8945053, U.S. PatentNo. 8939944, U.S. Patent No. 8834431,U.S. Patent No. 8827963, U.S. Patent No. 8758292, U.S. Patent No. 8734403, U.S. Patent No. 8721615,U.S. Patent No. 8690837, U.S. Patent No. 8679071, U.S. Patent No. 8672901, U.S. Patent No. 8657788,U.S. Patent No. 8647307, U.S. Patent No. 8591465, U.S. Patent No. 8562570, U.S. Patent No. 8556847,U.S. Patent No. 8491538, U.S. Patent No. 8439864, U.S. Patent No. 8409149, U.S. Patent No. 8409148,U.S. Patent No. 8409145, U.S. Patent No. 8398594, U.S. Patent No. 8398593, U.S. Patent No. 8343103,U.S. PatentNo. 8298175, U.S. Patent No. 8246577, U.S. Patent No. 8216180, U.S. Patent No. 8048037,U.S. Patent No. 8043262, U.S. Patent No. 8043249, U.S. Patent No. 8016797, U.S. Patent No. 7976509,U.S. Patent No. 7955303, U.S. Patent No. 7951113, U.S. Patent No. 7815598, U.S. Patent No. 7749186,U.S. Patent No. 7511480, U.S. Patent No. 7357790, PCT Publication No. W02023094119, PCT Publication No. WO2023072787, PCT Publication No. WO2023072728, PCT Publication No. WO2023062178, PCT Publication No. W02023057301, PCT Publication No. WO2023057272, PCT Publication No. WO2023051963, PCT Publication No. WO2023046741, PCT Publication No. WO2023046348, PCT Publication No. W02023017114, PCT Publication No. W02023012030, PCT Publication No. W02023001988, PCT Publication No. W02023001430, PCT Publication No. W02023001424, PCT Publication No. WO2023275273, PCT Publication No. WO2022268389, PCT Publication No. WO2022248119, PCT Publication No. WO2022248113, PCT Publication No. WO2022184539, PCT Publication No. WO2022184388, PCT Publication No. WO2022135921, PCT Publication No. WO2022128606, PCT Publication No. WO2022128385, PCT Publication No. WO2022106197, PCT Publication No. WO2022096352, PCT Publication No. W02022090047, PCT Publication No. WO2022069617, PCT Publication No. WO2022069175, PCT Publication No. WO2022058221, PCT Publication No. W02022053307, PCT Publication No. WO2022053248, PCT Publication No. WO2015127965, or PCT Publication No. WO2013170392, each of which is hereby incorporated by reference in its entirety.

[0092] Other devices that can be used to deliver injectables to a subject, including those that can handle larger volumes, include devices provided for in U.S. Patent No. 11833326, U.S. Patent No. 11786173, U.S. Patent No. 11744777, U.S. Patent No. 11571361, U.S. Patent No. 11571360, U.S. Patent No.11571164, U.S. Patent No. 11478583, U.S. Patent No. 11413393, U.S. Patent No. 11109800, U.S. Patent No. 11040138, U.S. Patent No. 11033680, U.S. Patent No. 10729842, U.S. Patent No. 10507285, U.S. Patent No. 10449293, U.S. Patent No. 9925333, U.S. Patent Application Publication No. 20230293108, U.S. Patent Application Publication No. 20230285243, U.S. Patent Application Publication No. 20230190582, U.S. Patent Application Publication No. 20230132382, U.S. Patent Application Publication No. 20230104373, U.S. Patent Application Publication No. 20220387705, U.S. Patent Application Publication No. 20220280385, U.S. Patent Application Publication No. 20220023533, U.S. Patent Application Publication No. 20210386621, U.S. Patent Application Publication No. 20210338928, U.S. Patent Application Publication No. 20200338257, U.S. Patent Application Publication No. 20200061292, U.S. Patent Application Publication No. 20180207369, PCT Publication No. WO2022031784, PCT Publication No. W02022006063, PCT Publication No. WO2021016567, PCT Publication No.WO2020142544, PCT Publication No. W02020118165, PCT Publication No. W02020086581, PCT Publication No. WO2019079335, PCT Publication No. WO2019075337, PCT Publication No.WO2018232171, PCT Publication No. WO2018218082, PCT Publication No. WO2018165588, PCT Publication No. WO2017014847, PCT Publication No. WO2016154413, or PCT Publication No. WO2016153747, each of which is hereby incorporated by reference in its entirety.

[0093] In some embodiments, one may administer the antibody in a local rather than systemic manner, for example, via injection of the antibody directly into an arthritic joint or pathogen-induced lesion characterized by immunopathology, often in a depot or sustained release formulation. Furthermore, one may administer the antibody in a targeted drug delivery system, for example, in a liposome coated with a tissue-specific antibody, targeting, for example, arthritic joint or pathogen-induced lesion characterized by immunopathology. Such liposomes are then targeted to and taken up selectively by the afflicted tissue.

[0094] In some embodiments, the administration regimen may depend on several factors, including the serum or tissue turnover rate of the therapeutic antibody, the level of symptoms, the immunogenicity of the therapeutic antibody, and / or the accessibility of the target cells in the biological matrix. Preferably, the administration regimen delivers sufficient therapeutic antibody to effect improvement in the target disease state, while simultaneously minimizing undesired side effects. Accordingly, the amount of biologic delivered depends in part on the particular therapeutic antibody and the severity of the condition being treated. Guidance in selecting appropriate doses of therapeutic antibodies is available (see, e.g, Wawrzynczak (1996) Antibody Therapy, Bios Scientific Pub. Ltd, Oxfordshire, UK; Kresina (ed.) (1991)Monoclonal Antibodies, Cytokines and Arthritis, Marcel Dekker, New York, NY; Bach (ed.) (1993) Monoclonal Antibodies and Peptide Therapy in Autoimmune Diseases, Marcel Dekker, New York, NY; Baert, et al. (2003) New Engl. J. Med. 348:601-608; Milgrom et al. (1999) New Engl. J. Med. 341 : 1966- 1973; Slamon et al. (2001) New Engl. J. Med. 344:783-792; Beniaminovitz et al. (2000) New Engl. J. Med. 342:613-619; Ghosh et al. (2003) New Engl. J. Med. 348:24-32; Lipsky et al. (2000) New Engl. J. Med. 343: 1594-1602).

[0095] Determination of the appropriate dose can be made by the clinician, e.g., using parameters or factors known or suspected in the art to affect treatment. Generally, the dose begins with an amount somewhat less than the optimum dose and it is increased by small increments thereafter until the desired or optimum effect is achieved relative to any negative side effects. Important diagnostic measures include those of symptoms of, e.g., the inflammation or level of inflammatory cytokines produced. In general, it is desirable that a biologic that will be used is derived from the same species as the animal targeted for treatment, thereby minimizing any immune response to the reagent. In the case of human subjects, for example, chimeric, humanized and fully human antibodies may be desirable.

[0096] In some embodiments, antibodies, or antigen binding fragments thereof, can be provided by continuous infusion, or by doses administered, e.g., daily, 1-7 times per week, weekly, bi-weekly, monthly, bimonthly, or quarterly. In some embodiments, a total weekly dose is generally at least 0.05 pg / kg body weight, more generally at least 0.2 pg / kg, 0.5 pg / kg, 1 pg / kg, 10 pg / kg, 100 pg / kg, 0.25 mg / kg,I.0 mg / kg, 2.0 mg / kg, 5.0 mg / mL, 10 mg / kg, 25 mg / kg, 50 mg / kg or more (see, e.g., Yang, et al. (2003) New Engl. J. Med. 349:427-434; Herold, etal. (2002)New Engl. J. Med. 346: 1692-1698; Liu, etal. (1999)J. Neurol. Neurosurg. Psych. 67:451-456; Portielji, et al. (20003) Cancer Immunol. Immunother. 52:133- 144). Doses may also be provided to achieve a pre-determined target concentration of the antibody in the subject’s serum, such as 0.1, 0.3, 1, 3, 10, 30, 100, 300, 400, 500, 600 pg / ml or more. In other embodiments, a fully human antibody is administered subcutaneously or intravenously, on a weekly, biweekly, every 4 weeks, monthly, bimonthly, or quarterly basis at 10, 20, 50, 80, 100, 200, 300, 400, 500, 600, 1000 or 2500 mg / subject.

[0097] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain; one or more of a buffer, an antioxidant, a sugar, a viscosity modifying agent, or a surfactant; and wherein the pharmaceuticalcomposition is at a pH of about 6.5 to about 8.0. In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0. In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0098] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 selected from any one HCDR1 provided herein, an HCDR2 selected from any one HCDR2 provided herein, and an HCDR3 selected from any one HCDR3 provided herein, and wherein the light chain comprises an LCDR1 selected from any one LCDR1 provided herein, an LCDR2 selected from any one LCDR2 provided herein, and an LCDR3 selected from any one LCDR3 provided herein; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0099] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 63, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 66; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0100] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 63, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 66; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0101] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 67, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 68; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0102] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 67, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 68; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0103] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 69, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 68; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mMof an antioxidant, about 1 % w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0104] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO:69, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 68; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0105] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO:70, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 71; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0106] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 70, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 71; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0107] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chaincomprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 72, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 71; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0108] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO:72, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 71; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0109] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO:73, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 71; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0110] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 73, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 71; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of aviscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0111] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 74, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 75; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0112] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 74, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 75; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0113] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 76, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 77; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0114] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO:76, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 77; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0115] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 78, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 79; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0116] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 78, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 79; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0117] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 80, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 81; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0118] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 61, an HCDR2 of SEQ ID NO: 62, and an HCDR3 of SEQ ID NO: 80, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 64, an LCDR2 of SEQ ID NO: 65, and an LCDR3 of SEQ ID NO: 81; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0119] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 84, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 87; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0120] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 84, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 87; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0121] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 88, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 89; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mMof an antioxidant, about 1 % w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0122] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 88, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 89; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0123] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 90, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 89; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0124] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 90, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 89; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0125] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chaincomprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 91, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 92; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0126] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 91, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 92; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0127] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 93, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 94; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0128] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 93, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 94; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of aviscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0129] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 84, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 95; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0130] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 84, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 95; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0131] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 96, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 97; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0132] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO:96, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 97; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0133] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 98, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 99; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0134] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 98, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 99; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0135] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 100, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 101; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0136] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 100, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 101; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0137] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 100, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 102; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0138] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 82, an HCDR2 of SEQ ID NO: 83, and an HCDR3 of SEQ ID NO: 100, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 85, an LCDR2 of SEQ ID NO: 86, and an LCDR3 of SEQ ID NO: 102; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0139] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 105, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 108; about 5 mM to about 50 mM of a buffer, about 5 mM toabout 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0140] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 105, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 108; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0141] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 109, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 110; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0142] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 109, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 110; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0143] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chaincomprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 111, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 112; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0144] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 111, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 112; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0145] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 105, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 113; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0146] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 105, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 113; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0147] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 114, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 115; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0148] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 114, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107 and an LCDR3 of SEQ ID NO: 115; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0149] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 116, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 113; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0150] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ IDNO: 116, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 113; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0151] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 117, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 103, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 118; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0152] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 117, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 103, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 118; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0153] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 116, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 119; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0154] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 116, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 119; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0155] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 120, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 121; about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0156] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 120, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 121; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0157] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 122, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 123; about 5 mM to about 50 mM of a buffer, about 5 mM toabout 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0158] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises an HCDR1 of SEQ ID NO: 103, an HCDR2 of SEQ ID NO: 104, and an HCDR3 of SEQ ID NO: 122, and wherein the light chain comprises an LCDR1 of SEQ ID NO: 106, an LCDR2 of SEQ ID NO: 107, and an LCDR3 of SEQ ID NO: 123; about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant; and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0159] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 1, and wherein the light chain variable region corresponds to SEQ ID NO: 2, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0160] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 1, and wherein the light chain variable region corresponds to SEQ ID NO: 2, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0161] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 3, and wherein the light chain variable region corresponds to SEQ ID NO: 4, about 5 mM to about 50 mM of a buffer, about 5 mM toabout 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0162] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 3, and wherein the light chain variable region corresponds to SEQ ID NO: 4, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0163] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 5, and wherein the light chain variable region corresponds to SEQ ID NO: 6, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0164] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 5, , and wherein the light chain variable region corresponds to SEQ ID NO: 6, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0165] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 7, and wherein the light chain variable region corresponds to SEQ ID NO: 8, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0166] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 7, and wherein the light chain variable region corresponds to SEQ ID NO: 8, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0167] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 9, and wherein the light chain variable region corresponds to SEQ ID NO: 10, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0168] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 9, and wherein the light chain variable region corresponds to SEQ ID NO: 10, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0169] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 11, and wherein the light chain variable region corresponds to SEQ ID NO: 12, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0170] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 11, and wherein the light chain variable region corresponds to SEQ ID NO: 12, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0171] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 13, and wherein the light chain variable region corresponds to SEQ ID NO: 14, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0172] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 13, and wherein the light chain variable region corresponds to SEQ ID NO: 14, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0173] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 15, and wherein the light chain variable region corresponds to SEQ ID NO: 16, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0174] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 15, and wherein the light chain variable region corresponds to SEQ ID NO: 16, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0175] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 17, and wherein the light chain variable region corresponds to SEQ ID NO: 18, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0176] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 17, and wherein the light chain variable region corresponds to SEQ ID NO: 18, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0177] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 19, and wherein the light chain variable region corresponds to SEQ ID NO: 20, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0178] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 19, and wherein the light chain variable region corresponds to SEQ ID NO: 20, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0179] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 21, and wherein the light chain variable region corresponds to SEQ ID NO: 22, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0180] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 21, and wherein the light chain variable region corresponds to SEQ ID NO: 22, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0181] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 23, and wherein the light chain variable region corresponds to SEQ ID NO: 24, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0182] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 23, and wherein the light chain variable region corresponds to SEQ ID NO: 24, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0183] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 25, and wherein the light chain variable region corresponds to SEQ ID NO: 26, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0184] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 25, and wherein the light chain variable region corresponds to SEQ ID NO: 26, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0185] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 27, and wherein the light chain variable region corresponds to SEQ ID NO: 28, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0186] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 27, and wherein the light chain variable region corresponds to SEQ ID NO: 28, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0187] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 29, and wherein the light chain variable region corresponds to SEQ ID NO: 30, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0188] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 29, and wherein the light chain variable region corresponds to SEQ ID NO: 30, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0189] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 31, and wherein the light chain variable region corresponds to SEQ ID NO: 32, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0190] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 31, and wherein the light chain variable region corresponds to SEQ ID NO: 32, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0191] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 33, and wherein the light chain variable region corresponds to SEQ ID NO: 34, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0192] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 33, and wherein the light chain variable region corresponds to SEQ ID NO: 34, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0193] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 35, and wherein the light chain variable region corresponds to SEQ ID NO: 36, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0194] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 35, and wherein the light chain variable region corresponds to SEQ ID NO: 36, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0195] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 37, and wherein the light chain variable region corresponds to SEQ ID NO: 38, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0196] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 37, and wherein the light chain variable region corresponds to SEQ ID NO: 38, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0197] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 39, and wherein the light chain variable region corresponds to SEQ ID NO: 40, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0198] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 39, and wherein the light chain variable region corresponds to SEQ ID NO: 40, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0199] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 41, and wherein the light chain variable region corresponds to SEQ ID NO: 42, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0200] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 41, and wherein the light chain variable region corresponds to SEQ ID NO: 42, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0201] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 43, and wherein the light chain variable region corresponds to SEQ ID NO: 44, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0202] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 43, and wherein the light chain variable region corresponds to SEQ ID NO: 44, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0203] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 45, and wherein the light chain variable region corresponds to SEQ ID NO: 46, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0204] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 45, and wherein the light chain variable region corresponds to SEQ ID NO: 46, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0205] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 47, and wherein the light chain variable region corresponds to SEQ ID NO: 48, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0206] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 47, and wherein the light chain variable region corresponds to SEQ ID NO: 48, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0207] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 49, and wherein the light chain variable region corresponds to SEQ ID NO: 50, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0208] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 49, and wherein the light chain variable region corresponds to SEQ ID NO: 50, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0209] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 51, and wherein the light chain variable region corresponds to SEQ ID NO: 52, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0210] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 51, and wherein the light chain variable region corresponds to SEQ ID NO: 52, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0211] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 53, and wherein the light chain variable region corresponds to SEQ ID NO: 54, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0212] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 53, and wherein the light chain variable region corresponds to SEQ ID NO: 54, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0213] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 55, and wherein the light chain variable region corresponds to SEQ ID NO: 56, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0214] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 55, and wherein the light chain variable region corresponds to SEQ ID NO: 56, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0215] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 57, and wherein the light chain variable region corresponds to SEQ ID NO: 58, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0216] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 57, and wherein the light chain variable region corresponds to SEQ ID NO: 58, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0217] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 59, and wherein the light chain variable region corresponds to SEQ ID NO: 60, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0218] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 59, and wherein the light chain variable region corresponds to SEQ ID NO: 60, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0219] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 334, and wherein the light chain variable region corresponds to SEQ ID NO: 2, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0220] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 334, and wherein the light chain variable region corresponds to SEQ ID NO: 2, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0221] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 335, and wherein the light chain variable region corresponds to SEQ ID NO: 4, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0222] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 335, and wherein the light chain variable region corresponds to SEQ ID NO: 4, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0223] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 336, and wherein the light chain variable region corresponds to SEQ ID NO: 6, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0224] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 336, and wherein the light chain variable region corresponds to SEQ ID NO: 6, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0225] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 337, and wherein the light chain variable region corresponds to SEQ ID NO: 8, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0226] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 337, and wherein the light chain variable region corresponds to SEQ ID NO: 8, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0227] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 338, and wherein the light chain variable region corresponds to SEQ ID NO: 10, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0228] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 338, and wherein the light chain variable region corresponds to SEQ ID NO: 10, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0229] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 339, and wherein the light chain variable region corresponds to SEQ ID NO: 12, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0230] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 339, and wherein the light chain variable region corresponds to SEQ ID NO: 12, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0231] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 340, and wherein the light chain variable region corresponds to SEQ ID NO: 14, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0232] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 340, and wherein the light chain variable region corresponds to SEQ ID NO: 14, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0233] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 341, and wherein the light chain variable region corresponds to SEQ ID NO: 16, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180I l lmM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0234] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 341, and wherein the light chain variable region corresponds to SEQ ID NO: 16, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0235] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 342, and wherein the light chain variable region corresponds to SEQ ID NO: 18, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0236] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 342, and wherein the light chain variable region corresponds to SEQ ID NO: 18, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0237] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 343, and wherein the light chain variable region corresponds to SEQ ID NO: 20, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0238] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 343, and wherein the light chain variable region corresponds to SEQ ID NO: 20, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0239] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 344, and wherein the light chain variable region corresponds to SEQ ID NO: 22, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0240] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 344, and wherein the light chain variable region corresponds to SEQ ID NO: 22, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0241] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 345, and wherein the light chain variable region corresponds to SEQ ID NO: 24, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0242] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 345, and wherein the light chain variable region corresponds to SEQ ID NO: 24, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0243] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 346, and wherein the light chain variable region corresponds to SEQ ID NO: 26, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0244] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 346, and wherein the light chain variable region corresponds to SEQ ID NO: 26, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0245] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 347, and wherein the light chain variable region corresponds to SEQ ID NO: 28, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0246] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 347, and wherein the light chain variable region corresponds to SEQ ID NO: 28, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0247] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 348, and wherein the light chain variable region corresponds to SEQ ID NO: 30, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0248] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 348, and wherein the light chain variable region corresponds to SEQ ID NO: 30, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0249] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 349, and wherein the light chain variable region corresponds to SEQ ID NO: 32, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0250] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 349, and wherein the light chain variable region corresponds to SEQ ID NO: 32, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0251] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 350, and wherein the light chain variable region corresponds to SEQ ID NO: 34, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0252] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 350, and wherein the light chain variable region corresponds to SEQ ID NO: 34, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0253] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 351, and wherein the light chain variable region corresponds to SEQ ID NO: 36, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0254] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 351, and wherein the light chain variable region corresponds to SEQ ID NO: 36, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0255] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 352, and wherein the light chain variable region corresponds to SEQ ID NO: 38, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0256] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 352, and wherein the light chain variable region corresponds to SEQ ID NO: 38, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0257] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 353, and wherein the light chain variable region corresponds to SEQ ID NO: 40, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0258] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 353, and wherein the light chain variable region corresponds to SEQ ID NO: 40, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0259] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 354, and wherein the light chain variable region corresponds to SEQ ID NO: 42, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0260] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 354, and wherein the light chain variable region corresponds to SEQ ID NO: 42, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0261] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 355, and wherein the light chain variable region corresponds to SEQ ID NO: 44, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0262] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 355, and wherein the light chain variable region corresponds to SEQ ID NO: 44, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0263] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 356, and wherein the light chain variable region corresponds to SEQ ID NO: 46, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0264] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 356, and wherein the light chain variable region corresponds to SEQ ID NO: 46, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0265] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 357, and wherein the light chain variable region corresponds to SEQ ID NO: 48, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0266] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 357, and wherein the light chain variable region corresponds to SEQ ID NO: 48, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0267] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 358, and wherein the light chain variable region corresponds to SEQ ID NO: 50, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0268] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 358, and wherein the light chain variable region corresponds to SEQ ID NO: 50, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0269] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 359, and wherein the light chain variable region corresponds to SEQ ID NO: 52, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0270] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 359, and wherein the light chain variable region corresponds to SEQ ID NO: 52, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0271] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 360, and wherein the light chain variable region corresponds to SEQ ID NO: 54, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0272] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 360, and wherein the light chain variable region corresponds to SEQ ID NO: 54, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0273] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 361, and wherein the light chain variable region corresponds to SEQ ID NO: 56, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0274] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 361, and wherein the light chain variable region corresponds to SEQ ID NO: 56, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0275] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 362, and wherein the light chain variable region corresponds to SEQ ID NO: 58, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0276] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 362, and wherein the light chain variable region corresponds to SEQ ID NO: 58, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0277] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 363, and wherein the light chain variable region corresponds to SEQ ID NO: 60, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0278] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region corresponds to SEQ ID NO: 363, and wherein the light chain variable region corresponds to SEQ ID NO: 60, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0279] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 168 or SEQ ID NO: 169, and the light chain corresponds to SEQ ID NO: 228, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0280] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 168 or SEQ ID NO: 169, and the light chain corresponds to SEQ ID NO: 228, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0281] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 170 or SEQ ID NO: 171, and the light chain corresponds to SEQ ID NO: 229, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0282] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 170 or SEQ ID NO: 171, and the light chain corresponds to SEQ ID NO:229, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0283] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 172 or SEQ ID NO: 173, and the light chain corresponds to SEQ ID NO:230, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0284] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 172 or SEQ ID NO: 173, and the light chain corresponds to SEQ ID NO:230, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0285] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 174 or SEQ ID NO: 175, and the light chain corresponds to SEQ ID NO:231, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0286] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 174 or SEQ ID NO: 175, and the light chain corresponds to SEQ ID NO:231, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0287] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 176 or SEQ ID NO: 177, and the light chain corresponds to SEQ ID NO:232, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0288] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 176 or SEQ ID NO: 177, and the light chain corresponds to SEQ ID NO:232, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0289] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 178 or SEQ ID NO: 179, and the light chain corresponds to SEQ ID NO:233, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0290] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 178 or SEQ ID NO: 179, and the light chain corresponds to SEQ ID NO:233, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0291] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 180 or SEQ ID NO: 181, and the light chain corresponds to SEQ ID NO:234, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0292] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 180 or SEQ ID NO: 181, and the light chain corresponds to SEQ ID NO:234, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0293] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 182 or SEQ ID NO: 183, and the light chain corresponds to SEQ ID NO:235, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0294] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 182 or SEQ ID NO: 183, and the light chain corresponds to SEQ ID NO:235, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0295] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 184 or SEQ ID NO: 185, and the light chain corresponds to SEQ ID NO:236, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0296] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 184 or SEQ ID NO: 185, and the light chain corresponds to SEQ ID NO:236, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0297] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 186 or SEQ ID NO: 187, and the light chain corresponds to SEQ ID NO:237, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0298] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 186 or SEQ ID NO: 187, and the light chain corresponds to SEQ ID NO:237, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0299] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 188 or SEQ ID NO: 189, and the light chain corresponds to SEQ ID NO:238, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0300] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 188 or SEQ ID NO: 189, and the light chain corresponds to SEQ ID NO:238, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0301] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 190 or SEQ ID NO: 191, and the light chain corresponds to SEQ ID NO:239, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0302] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 190 or SEQ ID NO: 191, and the light chain corresponds to SEQ ID NO:239, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0303] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 192 or SEQ ID NO: 193, and the light chain corresponds to SEQ ID NO:240, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0304] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 192 or SEQ ID NO: 193, and the light chain corresponds to SEQ ID NO:240, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0305] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 194 or SEQ ID NO: 195, and the light chain corresponds to SEQ ID NO:241, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0306] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 194 or SEQ ID NO: 195, and the light chain corresponds to SEQ ID NO:241, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0307] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 196 or SEQ ID NO: 197, and the light chain corresponds to SEQ ID NO:242, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0308] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 196 or SEQ ID NO: 197, and the light chain corresponds to SEQ ID NO:242, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0309] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 198 or SEQ ID NO: 199, and the light chain corresponds to SEQ ID NO:243, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0310] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 198 or SEQ ID NO: 199, and the light chain corresponds to SEQ ID NO:243, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0311] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 200 or SEQ ID NO: 201, and the light chain corresponds to SEQ ID NO:244, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0312] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 200 or SEQ ID NO: 201, and the light chain corresponds to SEQ ID NO:244, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0313] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 202 or SEQ ID NO: 203, and the light chain corresponds to SEQ ID NO:245, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0314] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 202 or SEQ ID NO: 203, and the light chain corresponds to SEQ ID NO:245, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0315] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 204 or SEQ ID NO: 205, and the light chain corresponds to SEQ ID NO:246, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0316] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 204 or SEQ ID NO: 205, and the light chain corresponds to SEQ ID NO:246, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0317] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 206 or SEQ ID NO: 207, and the light chain corresponds to SEQ ID NO:247, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0318] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 206 or SEQ ID NO: 207, and the light chain corresponds to SEQ ID NO:247, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0319] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 208 or SEQ ID NO: 209, and the light chain corresponds to SEQ ID NO:248, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0320] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 208 or SEQ ID NO: 209, and the light chain corresponds to SEQ ID NO:248, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0321] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 210 or SEQ ID NO: 211, and the light chain corresponds to SEQ ID NO:249, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0322] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 210 or SEQ ID NO: 211, and the light chain corresponds to SEQ ID NO:249, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0323] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 212 or SEQ ID NO: 213, and the light chain corresponds to SEQ ID NO:250, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0324] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 212 or SEQ ID NO: 213, and the light chain corresponds to SEQ ID NO:250, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0325] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 214 or SEQ ID NO: 215, and the light chain corresponds to SEQ ID NO:251, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0326] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 214 or SEQ ID NO: 215, and the light chain corresponds to SEQ ID NO:251, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0327] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 216 or SEQ ID NO: 217, and the light chain corresponds to SEQ ID NO:252, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0328] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 216 or SEQ ID NO: 217, and the light chain corresponds to SEQ ID NO:252, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0329] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 218 or SEQ ID NO: 219, and the light chain corresponds to SEQ ID NO:253, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0330] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 218 or SEQ ID NO: 219, and the light chain corresponds to SEQ ID NO:253, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0331] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 220 or SEQ ID NO: 221, and the light chain corresponds to SEQ ID NO:254, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0332] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 220 or SEQ ID NO: 221, and the light chain corresponds to SEQ ID NO:254, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0333] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 222 or SEQ ID NO: 223, and the light chain corresponds to SEQ ID NO:255, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0334] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 222 or SEQ ID NO: 223, and the light chain corresponds to SEQ ID NO:255, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0335] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 224 or SEQ ID NO: 225, and the light chain corresponds to SEQ ID NO:256, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0336] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 224 or SEQ ID NO: 225, and the light chain corresponds to SEQ ID NO:256, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0337] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 226 or SEQ ID NO: 227, and the light chain corresponds to SEQ ID NO:257, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0338] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 226 or SEQ ID NO: 227, and the light chain corresponds to SEQ ID NO: 257, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0339] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 364 or SEQ ID NO: 365, and the light chain corresponds to SEQ ID NO: 228, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0340] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 364 or SEQ ID NO: 365, and the light chain corresponds to SEQ ID NO:228, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0341] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 366 or SEQ ID NO: 367, and the light chain corresponds to SEQ ID NO:229, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0342] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 366 or SEQ ID NO: 367, and the light chain corresponds to SEQ ID NO:229, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0343] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 368 or SEQ ID NO: 369, and the light chain corresponds to SEQ ID NO:230, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0344] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 368 or SEQ ID NO: 369, and the light chain corresponds to SEQ ID NO:230, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0345] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 370 or SEQ ID NO: 371, and the light chain corresponds to SEQ ID NO:231, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0346] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 370 or SEQ ID NO: 371, and the light chain corresponds to SEQ ID NO:231, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0347] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 372 or SEQ ID NO: 373, and the light chain corresponds to SEQ ID NO:232, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0348] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 372 or SEQ ID NO: 373, and the light chain corresponds to SEQ ID NO:232, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0349] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 374 or SEQ ID NO: 375, and the light chain corresponds to SEQ ID NO:233, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0350] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 374 or SEQ ID NO: 375, and the light chain corresponds to SEQ ID NO:233, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0351] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 376 or SEQ ID NO: 377, and the light chain corresponds to SEQ ID NO:234, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0352] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 376 or SEQ ID NO: 377, and the light chain corresponds to SEQ ID NO:234, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0353] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 378 or SEQ ID NO: 379, and the light chain corresponds to SEQ ID NO:235, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0354] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 378 or SEQ ID NO: 379, and the light chain corresponds to SEQ ID NO:235, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0355] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 380 or SEQ ID NO: 381, and the light chain corresponds to SEQ ID NO:236, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0356] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 380 or SEQ ID NO: 381, and the light chain corresponds to SEQ ID NO:236, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0357] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 382 or SEQ ID NO: 383, and the light chain corresponds to SEQ ID NO:237, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0358] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 382 or SEQ ID NO: 383, and the light chain corresponds to SEQ ID NO:237, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0359] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 384 or SEQ ID NO: 385, and the light chain corresponds to SEQ ID NO:238, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0360] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 384 or SEQ ID NO: 385, and the light chain corresponds to SEQ ID NO:238, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0361] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 386 or SEQ ID NO: 387, and the light chain corresponds to SEQ ID NO:239, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0362] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 386 or SEQ ID NO: 387, and the light chain corresponds to SEQ ID NO:239, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0363] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 388 or SEQ ID NO: 389, and the light chain corresponds to SEQ ID NO:240, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0364] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 388 or SEQ ID NO: 389, and the light chain corresponds to SEQ ID NO:240, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0365] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 390 or SEQ ID NO: 391, and the light chain corresponds to SEQ ID NO:241, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0366] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 390 or SEQ ID NO: 391, and the light chain corresponds to SEQ ID NO:241, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0367] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 392 or SEQ ID NO: 393, and the light chain corresponds to SEQ ID NO:242, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0368] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 392 or SEQ ID NO: 393, and the light chain corresponds to SEQ ID NO:242, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0369] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 394 or SEQ ID NO: 395, and the light chain corresponds to SEQ ID NO:243, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0370] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 394 or SEQ ID NO: 395, and the light chain corresponds to SEQ ID NO:243, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0371] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 396 or SEQ ID NO: 397, and the light chain corresponds to SEQ ID NO:244, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0372] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 396 or SEQ ID NO: 397, and the light chain corresponds to SEQ ID NO:244, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0373] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 398 or SEQ ID NO: 399, and the light chain corresponds to SEQ ID NO:245, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0374] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 398 or SEQ ID NO: 399, and the light chain corresponds to SEQ ID NO:245, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0375] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 400 or SEQ ID NO: 401, and the light chain corresponds to SEQ ID NO:246, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0376] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 400 or SEQ ID NO: 401, and the light chain corresponds to SEQ ID NO:246, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0377] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 402 or SEQ ID NO: 403, and the light chain corresponds to SEQ ID NO:247, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0378] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 402 or SEQ ID NO: 403, and the light chain corresponds to SEQ ID NO:247, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0379] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 404 or SEQ ID NO: 405, and the light chain corresponds to SEQ ID NO:248, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0380] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 404 or SEQ ID NO: 405, and the light chain corresponds to SEQ ID NO:248, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0381] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 406 or SEQ ID NO: 407, and the light chain corresponds to SEQ ID NO:249, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0382] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 406 or SEQ ID NO: 407, and the light chain corresponds to SEQ ID NO:249, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0383] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 408 or SEQ ID NO: 409, and the light chain corresponds to SEQ ID NO:250, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0384] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 408 or SEQ ID NO: 409, and the light chain corresponds to SEQ ID NO:250, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0385] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 410 or SEQ ID NO: 411, and the light chain corresponds to SEQ ID NO:251, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0386] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 410 or SEQ ID NO: 411, and the light chain corresponds to SEQ ID NO:251, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0387] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 412 or SEQ ID NO: 413, and the light chain corresponds to SEQ ID NO:252, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0388] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 412 or SEQ ID NO: 413, and the light chain corresponds to SEQ ID NO:252, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0389] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 414 or SEQ ID NO: 415, and the light chain corresponds to SEQ ID NO:253, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0390] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 414 or SEQ ID NO: 415, and the light chain corresponds to SEQ ID NO:253, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0391] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 416 or SEQ ID NO: 417, and the light chain corresponds to SEQ ID NO:254, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0392] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 416 or SEQ ID NO: 417, and the light chain corresponds to SEQ ID NO:254, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0393] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 418 or SEQ ID NO: 419, and the light chain corresponds to SEQ ID NO:255, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0394] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 418 or SEQ ID NO: 419, and the light chain corresponds to SEQ ID NO:255, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0395] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 420 or SEQ ID NO: 421, and the light chain corresponds to SEQ ID NO:256, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about 0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0396] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 420 or SEQ ID NO: 421, and the light chain corresponds to SEQ ID NO:256, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0397] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 422 or SEQ ID NO: 423, and the light chain corresponds to SEQ ID NO:257, about 5 mM to about 50 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 14% w / v of a sugar, about 20 mM to about 180 mM of a viscosity modifying agent, about0.001% w / v to about 0.4 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0398] In some embodiments, a pharmaceutical composition is provided that comprises about 25 mg / mL to about 200 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain corresponds to SEQ ID NO: 422 or SEQ ID NO: 423, and the light chain corresponds to SEQ ID NO: 257, about 15 mM to about 25 mM of a buffer, about 5 mM to about 15 mM of an antioxidant, about 1% w / v to about 10% w / v of a sugar, about 60 mM to about 150 mM of a viscosity modifying agent, about 0.001% w / v to about 0.2 % w / v of a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

[0399] In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 5 mM to about 15 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 20 mM to about 25 mM.

[0400] In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 5 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 10 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 25 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 30 mM. In some embodiments, the pharmaceutical composition comprises abuffer at a concentration of about 35 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 40 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 45 mM. In some embodiments, the pharmaceutical composition comprises a buffer at a concentration of about 50 mM.

[0401] In some embodiments, the pharmaceutical compositions comprise a buffer (e.g., histidine, acetate, phosphate or citrate buffer) and / or a stabilizer agent (e.g. human albumin), etc., or a combination thereof. In some embodiments, the pharmaceutical compositions comprise one or more pharmaceutically acceptable carriers, including, e.g., ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, sucrose, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose- based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, polyethylene- polyoxypropylene-block polymers, and polyethylene glycol, or a combination thereof.

[0402] Various buffers can be present in the compositions of the present disclosure. In some embodiments, the pharmaceutical composition comprises a buffer, wherein the buffer is phosphoric acid buffer, citric acid buffer, acetic acid buffer, succinic acid buffer, citrate buffer, ascorbic acid buffer, glutamic acid buffer, lactic acid buffer, maleic acid buffer, trometamol buffer, and gluconic acid buffer, acetate buffer, succinate buffer, phosphate buffer, histidine buffer or any combination thereof. In some embodiments, the buffer is histidine buffer, histidine HC1 buffer, glycine buffer, Tris / glycine buffer, acetate buffer, sodium acetate buffer, potassium acetate buffer, magnesium acetate buffer, phosphate buffer, citrate buffer, or succinate buffer. In some embodiments, the buffer is histidine buffer. In some embodiments, the buffer is histidine HC1 buffer. In some embodiments, the buffer is glycine buffer. In some embodiments, the buffer is Tris / glycine buffer. In some embodiments, the buffer is acetate buffer. In some embodiments, the buffer is sodium acetate buffer. In some embodiments, the buffer is potassium acetate buffer. In some embodiments, the buffer is magnesium acetate buffer. In some embodiments, the buffer is phosphate buffer. In some embodiments, the buffer is citrate buffer. In some embodiments, the buffer is succinate buffer.

[0403] In some embodiments, the pharmaceutical composition comprises a buffer selected from tris buffer, histidine buffer, HEPES, phosphate buffer, acetate buffer, citrate buffer, succinate buffer, ascorbate buffer, glutamate buffer, lactate buffer, maleate buffer, trometamol buffer, gluconate buffer, or any combination thereof.

[0404] In some embodiments, the pharmaceutical composition comprises tris buffer. In some embodiments, the pharmaceutical composition comprises histidine buffer. In some embodiments, the pharmaceutical composition comprises HEPES. In some embodiments, the pharmaceutical composition comprises phosphate buffer. In some embodiments, the pharmaceutical composition comprises acetate buffer. In some embodiments, the pharmaceutical composition comprises citrate buffer. In some embodiments, the pharmaceutical composition comprises succinate buffer. In some embodiments, the pharmaceutical composition comprises ascorbate buffer. In some embodiments, the pharmaceutical composition comprises glutamate buffer. In some embodiments, the pharmaceutical composition comprises lactate buffer. In some embodiments, the pharmaceutical composition comprises maleate buffer. In some embodiments, the pharmaceutical composition comprises trometamol buffer. In some embodiments, the pharmaceutical composition comprises gluconate buffer.

[0405] In some embodiments, the pharmaceutical composition comprises a phosphate buffer. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 5 mM to about 15 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 20 mM to about 25 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 25 mM to about 50 mM.

[0406] In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at aconcentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises phosphate buffer at a concentration of about 25 mM.

[0407] In some embodiments, the pharmaceutical composition comprises a tris buffer. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 20 mM to about 25 mM.

[0408] In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises tris buffer at a concentration of about 25 mM.

[0409] In some embodiments, the pharmaceutical composition comprises a histidine buffer. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 20 mM to about 25 mM.

[0410] In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises histidine buffer at a concentration of about 25 mM.

[0411] In some embodiments, the pharmaceutical composition comprises HEPES. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 20 mM to about 25 mM.

[0412] In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises HEPES at a concentration of about 25 mM.

[0413] In some embodiments, the pharmaceutical composition comprises acetate buffer. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 20 mM to about 25 mM.

[0414] In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises acetate buffer at a concentration of about 25 mM.

[0415] In some embodiments, the pharmaceutical composition comprises citrate buffer. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 20 mM to about 25 mM.

[0416] In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 21 mM.In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises citrate buffer at a concentration of about 25 mM.

[0417] In some embodiments, the pharmaceutical composition comprises succinate buffer. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 20 mM to about 25 mM.

[0418] In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises succinate buffer at a concentration of about 25 mM.

[0419] In some embodiments, the pharmaceutical composition comprises ascorbate buffer. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 20 mM to about 25 mM.

[0420] In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprisesascorbate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises ascorbate buffer at a concentration of about 25 mM.

[0421] In some embodiments, the pharmaceutical composition comprises glutamate buffer. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 20 mM to about 25 mM.

[0422] In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises glutamate buffer at a concentration of about 25 mM.

[0423] In some embodiments, the pharmaceutical composition comprises lactate buffer. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 20 mM to about 25 mM.

[0424] In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises lactate buffer at a concentration of about 25 mM.

[0425] In some embodiments, the pharmaceutical composition comprises maleate buffer. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 20 mM to about 25 mM.

[0426] In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentrationof about 21 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises maleate buffer at a concentration of about 25 mM.

[0427] In some embodiments, the pharmaceutical composition comprises trometamol buffer. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 20 mM to about 25 mM.

[0428] In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises trometamol buffer at a concentration of about 25 mM.

[0429] In some embodiments, the pharmaceutical composition comprises gluconate buffer. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 15 mM to about 20 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 20 mM to about 25 mM.

[0430] In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 15 mM. In some embodiments, the pharmaceutical composition comprisesgluconate buffer at a concentration of about 16 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 17 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 18 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 19 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 20 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 21 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 22 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 23 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 24 mM. In some embodiments, the pharmaceutical composition comprises gluconate buffer at a concentration of about 25 mM.

[0431] In some embodiments, the pharmaceutical composition has a pH of about 6.5-8.0. In some embodiments, the pharmaceutical composition has a pH of about 6.5 to about 7.7.

[0432] In some embodiments, the pharmaceutical composition has a pH of about 6.5. In some embodiments, the pharmaceutical composition has a pH of about 6.6. In some embodiments, the pharmaceutical composition has a pH of about 6.7. In some embodiments, the pharmaceutical composition has a pH of about 6.8. In some embodiments, the pharmaceutical composition has a pH of about 6.9. In some embodiments, the pharmaceutical composition has a pH of about 7.0. In some embodiments, the pharmaceutical composition has a pH of about 7.1. In some embodiments, the pharmaceutical composition has a pH of about 7.2. In some embodiments, the pharmaceutical composition has a pH of about 7.3. In some embodiments, the pharmaceutical composition has a pH of about 7.4. In some embodiments, the pharmaceutical composition has a pH of about 7.5. In some embodiments, the pharmaceutical composition has a pH of about 7.6. In some embodiments, the pharmaceutical composition has a pH of about 7.7. In some embodiments, the pharmaceutical composition has a pH of about 7.8. In some embodiments, the pharmaceutical composition has a pH of about 7.9. In some embodiments, the pharmaceutical composition has a pH of about 8.0. In some embodiments, the pharmaceutical composition has a pH of 6.5. In some embodiments, the pharmaceutical composition has a pH of 6.6. In some embodiments, the pharmaceutical composition has a pH of about 6.7. In some embodiments, the pharmaceutical composition has a pH of 6.8. In some embodiments, the pharmaceutical composition has a pH of 6.9. In some embodiments, thepharmaceutical composition has a pH of about 7.0. In some embodiments, the pharmaceutical composition has a pH of 7.1. In some embodiments, the pharmaceutical composition has a pH of 7.2. In some embodiments, the pharmaceutical composition has a pH of about 7.3. In some embodiments, the pharmaceutical composition has a pH of 7.4. In some embodiments, the pharmaceutical composition has a pH of about 7.5. In some embodiments, the pharmaceutical composition has a pH of 7.6. In some embodiments, the pharmaceutical composition has a pH of 7.7. In some embodiments, the pharmaceutical composition has a pH of about 7.8. In some embodiments, the pharmaceutical composition has a pH of 7.9. In some embodiments, the pharmaceutical composition has a pH of about 8.0.

[0433] In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 5 mM to about 15 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 5 mM to about 10 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 10 mM to about 15 mM.

[0434] In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 5 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 6 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 7 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 8 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 9 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 10 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 11 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 12 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 13 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 14 mM. In some embodiments, the pharmaceutical composition comprises an antioxidant present at a concentration of about 15 mM.

[0435] In some embodiments, the antibody compositions of the present disclosure comprise methionine.Methionine is an essential amino acid that can be represented by the structure of:

[0436] Methionine, as used herein, includes the free base form of methionine, as well as any and all salts thereof. In some embodiments, methionine includes a pharmaceutically acceptable salt thereof, e.g, methionine hydrochloride. Methionine, as used herein, also includes all enantiomers (e.g, L-methionine and S-methionine), and any combination of enantiomers (e.g, 50% L-methionine and 50% S-methionine; 90%-100% L-methionine and 10%-0% S-methionine, and the like). In some embodiments, the term "methionine " includes greater than 99% L-methionine and less than 1% S-methionine. In some embodiments, the term "methionine " includes an enantomerically pure L-methionine. In some embodiments, methionine is a pharmaceutical grade methionine.

[0437] In some embodiments, the antibody compositions of the present disclosure comprise arginine. Arginine is a conditionally non-essential amino acid that can be represented by the structure of:

[0438] Arginine, as used herein, includes the free base form of arginine, as well as any and all salts thereof. In some embodiments, arginine includes a pharmaceutically acceptable salt thereof, c.g., arginine hydrochloride. Arginine, as used herein, also includes all enantiomers (e.g., L-arginine and S-arginine), and any combination of enantiomers (e.g, 50% L-arginine and 50% S-arginine; 90%-100% L-arginine and 10%-0% S-arginine, etc.). In some embodiments, the term "arginine" includes greater than 99% L- arginine and less than 1% S-arginine. In some embodiments, the term "arginine" includes an enantomerically pure L- arginine. In some embodiments, arginine is a pharmaceutical grade arginine.

[0439] Various concentrations of an antioxidant can be present in the compositions of the present disclosure. In some embodiments, the pharmaceutical composition comprises greater than 1 mM antioxidant, greater than 2 mM antioxidant, greater than 3 mM antioxidant, or greater than 4 mM antioxidant. In other aspects, the pharmaceutical composition comprises up to 5 mM antioxidant, up to 6 mM antioxidant, up to 7 mM antioxidant, up to 8 mM antioxidant, up to 9 mM antioxidant, up to 10 mM antioxidant, up to 11 mM antioxidant, up to 12 mM antioxidant, up to 13 mM antioxidant, up to 15 mMantioxidant, or up to 20 mM antioxidant. In other aspects, the pharmaceutical composition comprises about 1 mM to about 20 mM, about 1 mM to about 15 mM, about 1 mM to about 10 mM, about 1 mM to about 5 mM, about 5 mM to about 20 mM, about 5 mM to about 15 mM, about 5 mM to about 10 mM, about 7 mM to about 13 mM, or about 10 mM antioxidant. In some embodiments, the pharmaceutical composition comprises about 10 mM antioxidant. In some embodiments, the pharmaceutical composition comprises 10 mM antioxidant.

[0440] Various concentrations of methionine can be present in the compositions of the present disclosure. In some embodiments, the pharmaceutical composition comprises greater than 1 mM methionine, greater than 2 mM methionine, greater than 3 mM methionine, or greater than 4 mM methionine. In other aspects, the pharmaceutical composition comprises up to 5 mM methionine, up to 6 mM methionine, up to 7 mM methionine, up to 8 mM methionine, up to 9 mM methionine, up to 10 mM methionine, up to 11 mM methionine, up to 12 mM methionine, up to 13 mM methionine, up to 14 mM methionine, up to 15 mM methionine, or up to 20 mM methionine. In other aspects, the pharmaceutical composition comprises about 1 mM to about 20 mM, about 1 mM to about 15 mM, about 1 mM to about 10 mM, about 1 mM to about5 mM, about 5 mM to about 20 mM, about 5 mM to about 15 mM, about 5 mM to about 10 mM, about 7 mM to about 13 mM, or about 10 mM methionine. In some embodiments, the pharmaceutical composition comprises about 10 mM methionine. In some embodiments, the pharmaceutical composition comprises 10 mM methionine. In some embodiments, methionine is added in an amount sufficient to maintain osmolality of the pharmaceutical composition. In some embodiments, methionine is added in an amount sufficient to achieve a hyper-tonic solution.

[0441] Various concentrations of L-methionine can be present in the compositions of the present disclosure. In some embodiments, the pharmaceutical composition comprises greater than 1 mM L- methionine, greater than 2 mM L-methionine, greater than 3 mM L-methionine, or greater than 4 mM L- methionine. In other aspects, the pharmaceutical composition comprises up to 5 mM L-methionine, up to6 mM L-methionine, up to 7 mM L-methionine, up to 8 mM L-methionine, up to 9 mM L-methionine, up to 10 mM L-methionine, up to 11 mM L-methionine, up to 12 mM L-methionine, up to 13 mM L- methionine, up to 14 mM L-methionine, up to 15 mM L-methionine, or up to 20 mM L-methionine. In other aspects, the pharmaceutical composition comprises about 1 mM to about 20 mM, about 1 mM to about 15 mM, about 1 mM to about 10 mM, about 1 mM to about 5 mM, about 5 mM to about 20 mM, about 5 mM to about 15 mM, about 5 mM to about 10 mM, about 7 mM to about 13 mM, or about 10 mML-methionine. In some embodiments, the pharmaceutical composition comprises about 10 mM L- methionine. In some embodiments, the pharmaceutical composition comprises 10 mM L-methionine.

[0442] In some embodiments, the antioxidant is L-methionine. In some embodiments the antioxidant is ascorbic acid. In some embodiments, the antioxidant is EDTA.

[0443] In some embodiments, the pharmaceutical composition comprises L-methionine present at about 5 mM to about 15 mM. In some embodiments, the pharmaceutical composition comprises L-methionine present at a concentration of about 5 mM to about 10 mM. In some embodimen...

Claims

WHAT IS CLAIMED:

1. A pharmaceutical composition comprising: about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises a HCDR1 of SEQ ID NO: 61, a HCDR2 of SEQ ID NO: 62, and a HCDR3 of SEQ ID NO: 78, and wherein the light chain comprises a LCDR1 of SEQ ID NO: 64, a LCDR2 of SEQ ID NO: 65, and a LCDR3 of SEQ ID NO: 79; one or more of a buffer; an antioxidant; a sugar; a viscosity modifying agent; a surfactant, and wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.2 The pharmaceutical composition of claim 1, wherein the pharmaceutical composition comprises: a buffer at about 5 mM to about 50 mM; an antioxidant at about 5 mM to about 15 mM; a sugar at about 1% w / v to about 14% w / v; a viscosity modifying agent at about 20 mM to about 180 mM; and a surfactant at about 0.001 % w / v to about 0.4 % w / v.3 The pharmaceutical composition of claim 1, wherein the pharmaceutical composition comprises: a buffer at about 15 mM to about 25 mM; an antioxidant at about 5 mM to about 15 mM; a sugar at about 1% w / v to about 10% w / v; a viscosity modifying agent at about 60 mM to about 150 mM; and a surfactant at about 0.001 % w / v to about 0.2 % w / v.4 The pharmaceutical composition of claim 1, wherein the buffer is at a concentration of about 5 mM to about 15 mM, about 15 mM to about 20 mM, about 20 mM to about 25 mM, about 25 mM to about 30 mM, about 30 mM to about 35 mM, about 35 mM to about 40 mM, about 40 mM to about 45 mM, about45 mM to about 50 mM, about 5 mM, about 10 mM, about 15 mM, about 20 mM, about 25 mM, about 30 mM, about 35 mM, about 40 mM, about 45 mM, or about 50 mM.

5. The pharmaceutical composition of claim 4, wherein the buffer is present at a concentration of about 20 mM.

6. The pharmaceutical composition of any one of claims 1-5, wherein the buffer is selected from tris buffer, histidine buffer, HEPES, phosphate buffer, acetate buffer, citrate buffer, succinate buffer, ascorbate buffer, glutamate buffer, lactate buffer, maleate buffer, trometamol buffer, gluconate buffer, or any combination thereof.

7. The pharmaceutical composition of any one of claims 1-6, wherein the buffer is a phosphate buffer.

8. The pharmaceutical composition of claim 1, wherein the pharmaceutical composition has a pH of about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about7.5, about 7.6, about 7.7, about 7.8, about 7.9, or about 8.0.

9. The pharmaceutical composition of claim 1-8, wherein the pharmaceutical composition has a pH of about 6.5 to about 7.7.

10. The pharmaceutical composition of any one of claims 1-9, wherein the pharmaceutical composition has a pH of about 7.2.

11. The pharmaceutical composition of claim 1, wherein the antioxidant is present at about 10 mM to about 15 mM, or about 5 mM to about 10 mM.

12. The pharmaceutical composition of any one of claims 1-11, wherein the antioxidant is present at a concentration of about 10 mM.

13. The pharmaceutical composition of any one of claims 1-12, wherein the antioxidant is selected from L-methionine, ascorbic acid, EDTA, or any combination thereof.

14. The pharmaceutical composition of claim 13, wherein the antioxidant is L-methionine.

15. The pharmaceutical composition of claim 1, wherein the sugar is present at a concentration of about 1% w / v to about 14% w / v, about 2% w / v to about 14% w / v, about 2% w / v to about 12% w / v, 2% w / v to about 10% w / v, about 2% w / v to about 8% w / v, about 2% w / v to about 6% w / v, about 2% w / v to about 4 w / v, about 4% w / v to about 14% w / v, about 4% w / v to about 12% w / v, about 4% w / v to about 10% w / v, about 4% w / v to about 8% w / v, about 4% w / v to about 6% w / v, about 6% w / v to about 14% w / v, about 6% w / v to about 12% w / v, about 6% w / v to about 10% w / v, about 6% w / v to about 8% w / v, about 8 w / v to about 14% w / v, about 8% w / v to about 12% w / v, about 8% w / v to about 10% w / v, about 10% / v to about 14% w / v, about 10% w / v to about 12% w / v, or about 12% w / v to about 14% w / v.16 The pharmaceutical composition of claim 15, wherein the sugar is present at a concentration of about 1 to about 14% w / v.17 The pharmaceutical composition of claim 16, wherein the sugar is present at a concentration of about 2 w / v to about 10% w / v.18 The pharmaceutical composition of any one of claims 15-17, wherein the sugar is present at a concentration of about 4% w / v.19 The pharmaceutical composition of any one of claims 15-18, wherein the sugar is present at a concentration of about 3.5% w / v.20 The pharmaceutical composition of any one of claims 1-19, wherein the sugar is sucrose, trehalose, sorbitol, mannitol, or any combination thereof.21 The pharmaceutical composition of any one of claims 1-20, wherein the sugar is sucrose.22 The pharmaceutical composition of claim 1, wherein the viscosity modifying agent is present at a concentration of about 20 mM to about 180 mM, about 20 mM to about 170 mM, about 20 mM to about160 mM, about 20 mM to about 150 mM, about 20 mM to about 140 mM, about 20 mM to about 130 mM, about 20 mM to about 120 mM, about 20 mM to about 110 mM, about 20 mM to about 100 mM, about 20 mM to about 90 mM, about 20 mM to about 80 mM, about 20 mM to about 70 mM, about 20 mM to about 60 mM, about 20 mM to about 50 mM, about 20 mM to about 40 mM, about 40 mM to about180 mM, about 40 mM to about 170 mM, about 40 mM to about 160 mM, about 40 mM to about 150 mM, about 40 mM to about 140 mM, about 40 mM to about 130 mM, about 40 mM to about 120 mM, about 40 mM to about 110 mM, about 40 mM to about 100 mM, about 40 mM to about 90 mM, about 40 mM to about 80 mM, about 40 mM to about 70 mM, about 40 mM to about 60 mM, about 40 mM to about 50 mM, about 60 mM to about 180 mM, about 60 mM to about 170 mM, about 60 mM to about 160 mM, about 60 mM to about 150 mM, about 60 mM to about 140 mM, about 60 mM to about 130 mM, about 60 mM to about 120 mM, about 60 mM to about 110 mM, about 60 mM to about 100 mM, about 60 mMo about 90 mM, about 60 mM to about 80 mM, about 60 mM to about 70 mM, about 70 mM to about180 mM, about 70 mM to about 170 mM, about 70 mM to about 160 mM, about 70 mM to about 150 mM, about 70 mM to about 140 mM, about 70 mM to about 130 mM, about 70 mM to about 120 mM, about 70 mM to about 110 mM, about 70 mM to about 100 mM, about 70 mM to about 90 mM, about 70 mM to about 80 mM, about 80 mM to about 180 mM, about 80 mM to about 170 mM, about 80 mM to about 160 mM, about 80 mM to about 150 mM, about 80 mM to about 140 mM, about 80 mM to about 130 mM, about 80 mM to about 120 mM, about 80 mM to about 110 mM, about 80 mM to about 100 mM, about 80 mM to about 90 mM, about 90 mM to about 180 mM, about 90 mM to about 170 mM, about 90 mM to about 160 mM, about 90 mM to about 150 mM, about 90 mM to about 140 mM, about 90 mM to about 130 mM, about 90 mM to about 120 mM, about 90 mM to about 110 mM, about 90 mMo about 100 mM, about 100 mM to about 180 mM, about 100 mM to about 170 mM, about 100 mM to about 160 mM, about 100 mM to about 150 mM, about 100 mM to about 140 mM, about 100 mM to about 130 mM, about 100 mM to about 120 mM, about 100 mM to about 110 mM, about 110 mM to about 180 mM, about 110 mM to about 170 mM, about 110 mM to about 160 mM, about 110 mM to about 150 mM, about 110 mM to about 140 mM, about 110 mM to about 130 mM, about 110 mM to about 120 mM, about 120 mM to about 180 mM, about 120 mM to about 170 mM, about 120 mM to about 160 mM, about 120 mM to about 150 mM, about 120 mM to about 140 mM, about 120 mM to about 130 mM, about 130 mM to about 180 mM, about 130 mM to about 170 mM, about 130 mM to about 160 mM, about 130 mM to about 150 mM, about 130 mM to about 140 mM, about 140 mM to about 180 mM, about 140 mM to about 170 mM, about 140 mM to about 160 mM, about 140 mM toabout 150 mM, about 150 mM to about 180 mM, about 150 mM to about 170 mM, about 150 mM to about 160 mM, about 160 mM to about 180 mM, about 160 mM to about 170 mM, or about 170 mM to about 180 mM.

23. The pharmaceutical composition of any one of claims 1-22, wherein the viscosity modifying agent is present at a concentration of about 70 mM.

24. The pharmaceutical composition of any one of claims 1-23, wherein the viscosity modifying agent is L-arginine hydrochloride (L-Arg-HCL) or sodium chloride (NaCl).

25. The pharmaceutical composition of any one of claims 1-24, wherein the viscosity modifying agent is L-Arg-HCL26. The pharmaceutical composition of claim 1, wherein the surfactant is present at a concentration of about 0.001% w / v to about 0.1% w / v, about 0.001% w / v to about 0.2% w / v, about 0.01% w / v to about 0.2% w / v, about 0.1% w / v to about 0.2% w / v, about 0.2% w / v to about 0.4% w / v, about 0.05% w / v to about 0.15% w / v, or about 0.001% w / v to about 0.01% w / v.

27. The pharmaceutical composition of any one of claims 1-26, wherein the surfactant is present at a concentration of about 0.1% w / v.

28. The pharmaceutical composition of any one of claims 1-27, wherein the surfactant is Polysorbate 80, Polysorbate 20, polyethylene glycol 3350 (PEG3350), or Poloxamer (P)188.

29. The pharmaceutical composition of any one of claims 1-28, wherein the surfactant is P188.

30. The pharmaceutical composition of claim 1, wherein the antibody is present at a concentration of about 25 mg / mL to about 300 mg / mL, about 25 mg / mL to about 275 mg / mL, about 25 mg / mL to about 250 mg / mL, about 25 mg / mL to about 225 mg / mL, about 25 mg / mL to about 200 mg / mL, about 25 mg / mL to about 175 mg / mL, about 25 mg / mL to about 150 mg / mL, about 25 mg / mL to about 125 mg / mL, about 25 mg / mL to about 100 mg / mL, about 25 mg / mL to about 75 mg / mL, about 50 mg / mL to about 300mg / mL, about 50 mg / mL to about 275 mg / mL, about 50 mg / mL to about 250 mg / mL, about 50 mg / mL to about 225 mg / mL, about 50 mg / mL to about 200 mg / mL, about 50 mg / mL to about 175 mg / mL, about 50 mg / mL to about 150 mg / mL, about 50 mg / mL to about 125 mg / mL, about 50 mg / mL to about 100 mg / mL, about 50 mg / mL to about 75 mg / mL, about 75 mg / mL to about 300 mg / mL, about 75 mg / mL to about 275 mg / mL, about 75 mg / mL to about 250 mg / mL, about 75 mg / mL to about 225 mg / mL, about 75 mg / mL to about 200 mg / mL, about 75 mg / mL to about 175 mg / mL, about 75 mg / mL to about 150 mg / mL, about 75 mg / mL to about 125 mg / mL, about 75 mg / mL to about 100 mg / mL, about 100 mg / mL to about 300 mg / mL, about 100 mg / mL to about 275 mg / mL, about 100 mg / mL to about 250 mg / mL, about 100 mg / mL to about 225 mg / mL, about 100 mg / mL to about 200 mg / mL, about 100 mg / mL to about 175 mg / mL, about 100 mg / mL to about 150 mg / mL, about 100 mg / mL to about 125 mg / mL, about 125 mg / mL to about 300 mg / mL, about 125 mg / mL to about 275 mg / mL, about 125 mg / mL to about 250 mg / mL, about 125 mg / mL to about 225 mg / mL, about 125 mg / mL to about 200 mg / mL, about 125 mg / mL to about 175 mg / mL, about 125 mg / mL to about 150 mg / mL, about 150 mg / mL to about 300 mg / mL, about 150 mg / mL to about 275 mg / mL, about 150 mg / mL to about 250 mg / mL, about 150 mg / mL to about 225 mg / mL, about 150 mg / mL to about 200 mg / mL, about 150 mg / mL to about 175 mg / mL, about 175 mg / mL to about 300 mg / mL, about 175 mg / mL to about 275 mg / mL, about 175 mg / mL to about 250 mg / mL, about 175 mg / mL to about 225 mg / mL, about 175 mg / mL to about 200 mg / mL, about 200 mg / mL to about 300 mg / mL, about 200 mg / mL to about 275 mg / mL, about 200 mg / mL to about 250 mg / mL, about 200 mg / mL to about 225 mg / mL, about 225 mg / mL to about 300 mg / mL, about 225 mg / mL to about 275 mg / mL, about 225 mg / mL to about 250 mg / mL, about 250 mg / mL to about 300 mg / mL, about 250 mg / mL to about 275 mg / mL, about 275 mg / mL to about 300 mg / mL, about 100 mg / mL to about 200 mg / mL, or about 200 mg / mL to about 300 mg / mL.

31. The pharmaceutical composition of any one of claim 1-30, wherein the antibody is present at a concentration of about 150 mg / mL.

32. The pharmaceutical composition of any one of claim 1-31, wherein the antibody is present at a concentration of about 100 mg / mL.

33. The pharmaceutical composition of any one of claim 1-32, wherein the antibody is a monoclonal antibody.

34. The pharmaceutical composition of any one of claim 1-33, wherein the monoclonal antibody is an immunoglobulin G4 (IgG4) type monoclonal antibody.

35. The pharmaceutical composition of claim 1, wherein the antibody comprises a heavy chain variable region with an amino acid sequence of SEQ ID NO: 17; and a light chain variable region with an amino acid sequence of SEQ ID NO: 18.

36. The pharmaceutical composition of claim 1, wherein the antibody comprises a heavy chain variable region with an amino acid sequence of SEQ ID NO: 342; and a light chain variable region with an amino acid sequence of SEQ ID NO: 18.

37. The pharmaceutical composition of any one of claims 1-36, wherein the antibody, or antibody fragment thereof, comprises a heavy chain variable region comprising heavy chain HCDR1, HCDR2, and HCDR3 sequences, wherein the heavy chain HCDR1 sequence has the amino acid sequence of SEQ ID NO: 61; the heavy chain HCDR2 has the amino acid sequence of SEQ ID NO: 62; and the heavy chain HCDR3 sequence has the amino acid sequence of SEQ ID NO: 78, or variants or convention equivalents of any of the foregoing; and (ii) a light chain variable region comprising light chain LCDR1, LCDR2, and LCDR3 sequences, wherein the light chain LCDR1 sequence has the amino acid sequence SEQ ID NO: 64; the light chain LCDR2 sequence has the amino acid sequence of SEQ ID NO: 65; and the light chain LCDR3 sequence has the amino acid sequence of SEQ ID NO: 79; or variants or convention equivalents of any of the foregoing.

38. The pharmaceutical composition of any one of claims 1-37, wherein the pharmaceutical composition is stable at about-25 °C, about -20 °C, about -15 °C, about -5 °C, about 0 °C, about 5 °C, or about 10 °C.

39. The pharmaceutical composition of any one of claims 1-38, wherein the pharmaceutical composition is stable for 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 13 months, 14 months, 15 months, 16 months, 17 months, 18 months, 19 months, 20 months, 21 months, 22 months, 23 months, 24 months, 25 months, 26 months, 27 months, 28 months, 29 months, 30 months, 31 months, 32 months, 33 months, 34months, 35 months, or 36 months.

40. The pharmaceutical composition of any one of claims 1-39, wherein the pharmaceutical composition is stable at -20 °C for at least 3 months.

41. The pharmaceutical composition of any one of claims 1-40, wherein the pharmaceutical composition is stable at -20 °C for at least 6 months.

42. The pharmaceutical composition of any one of claims 1-41, wherein the pharmaceutical composition is stable at 2-8 °C for at least 3 months.

43. The pharmaceutical composition of any one of claims 1-42, wherein the pharmaceutical composition is stable at 2-8 °C for at least 6 months.

44. The pharmaceutical composition of any one of claims 1-43, wherein the pharmaceutical composition is stable at 2-8 °C for at least 9 months.

45. The pharmaceutical composition of any one of claims 1-44, wherein the pharmaceutical composition is stored in pre-filled syringes or 2 mL aliquots in 6 mb vials.

46. The pharmaceutical composition of any one of claims 1-45, wherein the pharmaceutical composition is stored in 2 mL aliquots in 6 mL vials with a 20 mm stopper.

47. The pharmaceutical composition of any one of claims 1-46, wherein the pharmaceutical composition is stored in 2 mL aliquots at-20 °C in 6 mL vials with a 20 mm stopper and a 20 mm aluminum plastic cover.

48. The pharmaceutical composition of any one of claims 1-47, wherein the pharmaceutical composition is for intravenous or subcutaneous injection.

49. The pharmaceutical composition of any one of claims 1-48, wherein:the antibody is at about 100 mg / mL; the buffer is phosphate buffer at about 20 mM; the antioxidant is L-methionine at about 10 mM; the sugar is sucrose at about 4% w / v; the viscosity modifying agent is L-arginine hydrochloride at about 70 mM; and the surfactant is Pl 88 at about 0.1 % w / v, wherein the pharmaceutical composition is at a pH of about 7.2.

50. The pharmaceutical composition of any one of claims 1-49, wherein: the antibody is at about 150 mg / mL; the buffer is phosphate buffer at about 20 mM; the antioxidant is L-methionine at about 10 mM; the sugar is sucrose at about 3.5% w / v; the viscosity modifying agent is L-arginine hydrochloride at about 70 mM; and the surfactant is Pl 88 at about 0.1 % w / v, wherein the pharmaceutical composition is at a pH of about 7.2.

51. The pharmaceutical composition of any one of claims 1-50, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 0.2% after 24 months at a temperature of about -70 °C, relative to the initial value.

52. The pharmaceutical composition of any one of claims 1-50, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 0.4% after 24 months at a temperature of about -20 °C, relative to the initial value.

53. The pharmaceutical composition of any one of claims 1-50, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 0.5% after 6 months at a temperature of about 5 °C, relative to the initial value.

54. The pharmaceutical composition of any one of claims 1-50, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 3% after 6 months at atemperature of about 25 °C, relative to the initial value.

55. The pharmaceutical composition of any one of claims 1-50, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 7.8% after 1 month at a temperature of about 40 °C, relative to the initial value.

56. The pharmaceutical composition of any one of claims 1-50, wherein the main peak as measured by CE-SDS under non-reducing conditions is greater than 98% when stored at -20 C for up to 1, 3, 6, 9, 18, or 24 months.

57. The pharmaceutical composition of any one of claims 1-50, wherein the percentage of low molecular weight species (LMWS) as measured by CE-SDS under non-reducing conditions is less than, or about, 1.5, 1.1, or 1.0 % when stored at -20 C for up to 1, 3, 6, 9, 18, or 24 months.

58. The pharmaceutical composition of any one of claims 1-50, wherein the percentage of high molecular weight species (HMWS) as measured by SEC is less than 2.0% when stored at -20 C for up to 1, 3, 6, 9, 18, or 24 months.

59. The pharmaceutical composition of any one of claims 1-50, wherein the main peak as measured by CE-SDS under non-reducing conditions is greater than 97% when stored at 5 C for up to 1, 3, 6, 9, 18, or 24 months.

60. The pharmaceutical composition of any one of claims 1-50, wherein the percentage of low molecular weight species (LMWS) as measured by CE-SDS under non-reducing conditions is less than, or about, 2.5%, 2.0%, or 1.7% when stored at 5 C for up to 1, 3, 6, 9, 18, or 24 months.

61. The pharmaceutical composition of any one of claims 1-50, wherein the percentage of high molecular weight species (HMWS) as measured by SEC is less than 2.0% when stored at 5 C for up to 1, 3, 6, 9, 18, or 24 months.

62. The pharmaceutical composition of any one of claims 1-50, wherein the main peak as measuredby CE-SDS under non-reducing conditions is greater than 93% when stored at 25 C for up to 1, 3, 6, 9, 18, or 24 months.

63. The pharmaceutical composition of any one of claims 1-50, wherein the percentage of low molecular weight species (LMWS) as measured by CE-SDS under non-reducing conditions is less than, or about, 5%, 3.5%, or 1.5% when stored at 25 C for up to 1, 3, 6, 9, 18, or 24 months.

64. The pharmaceutical composition of any one of claims 1-50, wherein the percentage of high molecular weight species (HMWS) as measured by SEC is less than 5%, 3.5%, or 1.5% when stored at 25 C for up to 1, 3, 6, 9, 18, or 24 months.

65. A pharmaceutical composition comprising: about 25 mg / mL to about 300 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises a HCDR1 of SEQ ID NO: 61, a HCDR2 of SEQ ID NO: 62, and a HCDR3 of SEQ ID NO: 78, and wherein the light chain comprises a LCDR1 of SEQ ID NO: 64, a LCDR2 of SEQ ID NO: 65, and a LCDR3 of SEQ ID NO: 79; a buffer at about 15 mM to about 25 mM; an antioxidant at about 5 mM to about 15 mM; a sugar at about 1% w / v to about 10% w / v; a viscosity modifying agent at about 60 mM to about 150 mM; and a surfactant at about 0.001 % w / v to about 0.2 % w / v, wherein the pharmaceutical composition is at a pH of about 6.5 to about 8.0.

66. The pharmaceutical composition of claim 65, wherein the buffer is at a concentration of about 15 mM, about 20 mM, or about 25 mM.

67. The pharmaceutical composition of claim 65, wherein the buffer is at a concentration of about 20 mM.

68. The pharmaceutical composition of claim 65, wherein the buffer is selected from tris buffer, histidine uffer, HEPES, phosphate buffer, acetate buffer, citrate buffer, succinate buffer, ascorbate buffer,glutamate buffer, lactate buffer, maleate buffer, trometamol buffer, gluconate buffer, or any combination thereof.

69. The pharmaceutical composition of any one of claims 65-68, wherein the buffer is a phosphate buffer.

70. The pharmaceutical composition of claim 65, wherein the pharmaceutical composition has a pH of about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, about 7.6, about 7.7, about 7.8, about 7.9, or about 8.0.

71. The pharmaceutical composition of any one of claims 65-70, wherein the pharmaceutical composition has a pH of about 6.5 to about 7.7.

72. The pharmaceutical composition of claim 65, wherein the antioxidant is present at about 10 mM to about 15 mM, or about 5 mM to about 10 mM.

73. The pharmaceutical composition of any one of claims 65-72, wherein the antioxidant is present at a concentration of about 10 mM.

74. The pharmaceutical composition of any one of claims 65-73, wherein the antioxidant is selected from -methionine, ascorbic acid, EDTA, or any combination thereof.

75. The pharmaceutical composition of any one of claims 65-74, wherein the antioxidant is L-methionine.

76. The pharmaceutical composition of claim 65, wherein the sugar is present at a concentration of about 2 w / v to about 10% w / v.77 The pharmaceutical composition of any one of claims 65-76, wherein the sugar is present at a concentration of about 4% w / v.78 The pharmaceutical composition of any one of claims 65-77, wherein the sugar is present at a concentration of about 3.5% w / v.

79. The pharmaceutical composition of any one of claims 65-78, wherein the sugar is sucrose, trehalose, sorbitol, mannitol, or any combination thereof.

80. The pharmaceutical composition of any one of claims 65-79, wherein the sugar is sucrose.

81. The pharmaceutical composition of claim 65, wherein the viscosity modifying agent is present at a concentration of about 60 mM to about 150 mM, about 60 mM to about 140 mM, about 60 mM to about 130 mM, about 60 mM to about 120 mM, about 60 mM to about 110 mM, about 60 mM to about 100 mM, about 60 mM to about 90 mM, about 60 mM to about 80 mM, or about 60 mM to about 70 mM.

82. The pharmaceutical composition of any one of claims 65-81, wherein the viscosity modifying agent is present at a concentration of about 70 mM.

83. The pharmaceutical composition of any one of claims 65-82, wherein the viscosity modifying agent is L-arginine hydrochloride (L-Arg-HCL) or sodium chloride (NaCl).

84. The pharmaceutical composition of any one of claims 65-83, wherein the viscosity modifying agent is L-Arg-HCL.

85. The pharmaceutical composition of claim 65, wherein the surfactant is present at a concentration of about 0.001% w / v to about 0.1% w / v, about 0.001% w / v to about 0.2% w / v, about 0.01% w / v to about 0 2 w / v, about 0.1% w / v to about 0.2% w / v, about 0.2% w / v to about 0.4% w / v, about 0.05% w / v to about 0.15% w / v, or about 0.001% w / v to about 0.01% w / v.86 The pharmaceutical composition of any one of claims 65-85, wherein the surfactant is present at a concentration of about 0.1% w / v.87 The pharmaceutical composition of any one of claims 65-86, wherein the surfactant is Polysorbate 80, olysorbate 20, polyethylene glycol 3350 (PEG3350), or Poloxamer (P)188.

88. The pharmaceutical composition of any one of claims 65-87, wherein the surfactant is Pl 88.

89. The pharmaceutical composition of claim 65, wherein the antibody is present at a concentration of about 25 mg / mL to about 300 mg / mL, about 25 mg / mL to about 275 mg / mL, about 25 mg / mL to about 250 mg / mL, about 25 mg / mL to about 225 mg / mL, about 25 mg / mL to about 200 mg / mL, about 25 mg / mL to about 175 mg / mL, about 25 mg / mL to about 150 mg / mL, about 25 mg / mL to about 125 mg / mL, about 25 mg / mL to about 100 mg / mL, about 25 mg / mL to about 75 mg / mL, about 50 mg / mL to about 300 mg / mL, about 50 mg / mL to about 275 mg / mL, about 50 mg / mL to about 250 mg / mL, about 50 mg / mL to about 225 mg / mL, about 50 mg / mL to about 200 mg / mL, about 50 mg / mL to about 175 mg / mL, about 50 mg / mL to about 150 mg / mL, about 50 mg / mL to about 125 mg / mL, about 50 mg / mL to about 100 mg / mL, about 50 mg / mL to about 75 mg / mL, about 75 mg / mL to about 300 mg / mL, about 75 mg / mL to about 275 mg / mL, about 75 mg / mL to about 250 mg / mL, about 75 mg / mL to about 225 mg / mL, about 75 mg / mL to about 200 mg / mL, about 75 mg / mL to about 175 mg / mL, about 75 mg / mL to about 150 mg / mL, about 75 mg / mL to about 125 mg / mL, about 75 mg / mL to about 100 mg / mL, about 100 mg / mL to about 300 mg / mL, about 100 mg / mL to about 275 mg / mL, about 100 mg / mL to about 250 mg / mL, about 100 mg / mL to about 225 mg / mL, about 100 mg / mL to about 200 mg / mL, about 100 mg / mL to about 175 mg / mL, about 100 mg / mL to about 150 mg / mL, about 100 mg / mL to about 125 mg / mL, about 125 mg / mL to about 300 mg / mL, about 125 mg / mL to about 275 mg / mL, about 125 mg / mL to about 250 mg / mL, about 125 mg / mL to about 225 mg / mL, about 125 mg / mL to about 200 mg / mL, about 125 mg / mL to about 175 mg / mL, about 125 mg / mL to about 150 mg / mL, about 150 mg / mL to about 300 mg / mL, about 150 mg / mL to about 275 mg / mL, about 150 mg / mL to about 250 mg / mL, about 150 mg / mL to about 225 mg / mL, about 150 mg / mL to about 200 mg / mL, about 150 mg / mL to about 175 mg / mL, about 175 mg / mL to about 300 mg / mL, about 175 mg / mL to about 275 mg / mL, about 175 mg / mL to about 250 mg / mL, about 175 mg / mL to about 225 mg / mL, about 175 mg / mL to about 200 mg / mL, about 200 mg / mL to about 300 mg / mL, about 200 mg / mL to about 275 mg / mL, about 200 mg / mL to about 250 mg / mL, about 200 mg / mL to about 225 mg / mL, about 225 mg / mL to about 300 mg / mL, about 225 mg / mL to about 275 mg / mL, about 225 mg / mL to about 250 mg / mL, about 250 mg / mL to about 300 mg / mL, about 250 mg / mL to about 275 mg / mL, about 275 mg / mL to about 300 mg / mL, about 100 mg / mL to about 200 mg / mL, or about 200 mg / mL to about 300 mg / mL.

90. The pharmaceutical composition of any one of claims 65-89, wherein the antibody is present at aconcentration of about 150 mg / mL.

91. The pharmaceutical composition of any one of claims 65-90, wherein the antibody is present at a concentration of about 100 mg / mL.

92. The pharmaceutical composition of any one of claims 65-91, wherein the antibody is a monoclonal antibody.

93. The pharmaceutical composition of any one of claims 65-92, wherein the monoclonal antibody is an immunoglobulin G4 (IgG4) type monoclonal antibody.

94. The pharmaceutical composition of any one of claims 65-93, wherein the antibody comprises a heavy chain variable region with an amino acid sequence of SEQ ID NO: 17; and a light chain variable region with an amino acid sequence of SEQ ID NO: 18.

95. The pharmaceutical composition of any one of claims 65-94, wherein the antibody comprises a heavy chain variable region with an amino acid sequence of SEQ ID NO: 342; and a light chain variable region with an amino acid sequence of SEQ ID NO: 18.

96. The pharmaceutical composition of any one of claims 65-95, wherein the antibody, or antibody fragment thereof, comprises a heavy chain variable region comprising heavy chain HCDR1, HCDR2, and HCDR3 sequences, wherein the heavy chain HCDR1 sequence has the amino acid sequence of SEQ ID NO: 61; the heavy chain HCDR2 has the amino acid sequence of SEQ ID NO: 62; and the heavy chain HCDR3 sequence has the amino acid sequence of SEQ ID NO: 78, or variants or convention equivalents of any of the foregoing; and (ii) a light chain variable region comprising light chain LCDR1, LCDR2, and LCDR3 sequences, wherein the light chain LCDR1 sequence has the amino acid sequence SEQ ID NO: 64; the light chain LCDR2 sequence has the amino acid sequence of SEQ ID NO: 65; and the light chain LCDR3 sequence has the amino acid sequence of SEQ ID NO: 79; or variants or convention equivalents of any of the foregoing.

97. The pharmaceutical composition of any one of claims 65-96, wherein the pharmaceutical compositionis stable at about-25 °C, about -20 °C, about -15 °C, about -5 °C, about 0 °C, about 5 °C, or about 10 °C.

98. The pharmaceutical composition of any one of claims 65-97, wherein the pharmaceutical composition is stable for 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 7 months, 8 months, 9 months, 10 months, 11 months, 12 months, 13 months, 14 months, 15 months, 16 months, 17 months, 18 months, 19 months, 20 months, 21 months, 22 months, 23 months, or 24 months.

99. The pharmaceutical composition of any one of claims 65-98, wherein the pharmaceutical composition is stable at -20 °C for at least 3 months.

100. The pharmaceutical composition of any one of claims 65-99, wherein the pharmaceutical composition is stable at -20 °C for at least 6 months.

101. The pharmaceutical composition of any one of claims 65-100, wherein the pharmaceutical composition is stable at 2-8 °C for at least 3, 6 or 9 months.

102. The pharmaceutical composition of any one of claims 65-101, wherein: the antibody is at about 100 mg / mL; the buffer is phosphate buffer at about 20 mM; the antioxidant is L-methionine at about 10 mM; the sugar is sucrose at about 4% w / v; the viscosity modifying agent is L-arginine hydrochloride at about 70 mM; and the surfactant is Pl 88 at about 0.1 % w / v, wherein the pharmaceutical composition is at a pH of about 7.2.

103. The pharmaceutical composition of any one of claims 65-101, wherein: the antibody is at about 150 mg / mL; the buffer is phosphate buffer at about 20 mM; the antioxidant is L-methionine at about 10 mM; the sugar is sucrose at about 3.5% w / v; the viscosity modifying agent is L-arginine hydrochloride at about 70 mM; andthe surfactant is Pl 88 at about 0.1 % w / v, wherein the pharmaceutical composition is at a pH of about 7.2.

104. The pharmaceutical composition of any one of claims 65-103, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 0.2% after 24 months at a temperature of about -70 °C, relative to the initial value.

105. The pharmaceutical composition of any one of claims 65-103, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 0.4% after 24 months at a temperature of about -20 °C, relative to the initial value.

106. The pharmaceutical composition of any one of claims 65-103, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 0.5% after 6 months at a temperature of about 5 °C, relative to the initial value.

107. The pharmaceutical composition of any one of claims 65-103, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 3% after 6 months at aemperature of about 25 °C, relative to the initial value.

108. The pharmaceutical composition of any one of claims 65-103, wherein the pharmaceutical composition main peak, measured by SEC, decreases in area percent by less than 7.8% after 1 month at aemperature of about 40 °C, relative to the initial value.

109. A pharmaceutical composition comprising: about 150 mg / mL of an antibody having a heavy chain and a light chain, wherein the heavy chain comprises a HCDR1 of SEQ ID NO: 61, a HCDR2 of SEQ ID NO: 62, and a HCDR3 of SEQ ID NO: 78, and wherein the light chain comprises a LCDR1 of SEQ ID NO: 64, a LCDR2 of SEQ ID NO: 65, and a LCDR3 of SEQ ID NO: 79; the antibody is at about 150 mg / mL, the buffer is phosphate buffer at about 20 mM, the antioxidant is L-methionine at about 10 mM, the sugar is sucrose at about 3.5% w / v,the viscosity modifying agent is L-arginine hydrochloride at about 70 mM, and the surfactant is Pl 88 at about 0.1 % w / v; wherein the pharmaceutical composition is at a pH of about 7.2.

110. The pharmaceutical composition of claim 109, wherein the antibody comprises a heavy chain variable region with an amino acid sequence of SEQ ID NO: 17; and a light chain variable region with an amino acid sequence of SEQ ID NO: 18.

111. The pharmaceutical composition of claims 109 or 110, wherein the antibody comprises a heavy chain variable region with an amino acid sequence of SEQ ID NO: 342; and a light chain variable region with an amino acid sequence of SEQ ID NO: 18.

112. The pharmaceutical composition of any one of claims 109-111, wherein the antibody, or antibody fragment thereof, comprises a heavy chain variable region comprising heavy chain HCDR1, HCDR2, and HCDR3 sequences, wherein the heavy chain HCDR1 sequence has the amino acid sequence of SEQ ID NO: 61; the heavy chain HCDR2 has the amino acid sequence of SEQ ID NO: 62; and the heavy chain HCDR3 sequence has the amino acid sequence of SEQ ID NO: 78, or variants or convention equivalents of any of the foregoing; and (ii) a light chain variable region comprising light chain LCDR1, LCDR2, and LCDR3 sequences, wherein the light chain LCDR1 sequence has the amino acid sequence SEQ ID NO: 64; the light chain LCDR2 sequence has the amino acid sequence of SEQ ID NO: 65; and the light chain LCDR3 sequence has the amino acid sequence of SEQ ID NO: 79; or variants or convention equivalents of any of the foregoing.

113. A method of treating a subject with Cis mediated disorder, the method comprising administering to the subject the pharmaceutical composition of any one of claims 1-112.

114. The method of claim 1 13, wherein the Ci s Myasthenia Gravis, mediated disorder is hemolysis, Cold Agglutinin Disease, Immune Thrombocytopenia (ITP), Glomerulopathies, Atypical Hemolytic uremic syndrome, antiphospholipid antibody syndrome, transplant rejection, chronic inflammatory demyelinating polyneuropathy (CIDP), multifocal motor neuropathy (MMN), dermatomyositis, anti MAG neuropathy, due to stroke, or due to spinal cord injury.

115. The method of claims 113 or 114, wherein the volume of the pharmaceutical composition administered is about 1 mL or about 2 mL.

116. A kit comprising container a container comprising the pharmaceutical composition of any one of claims 1-112.

117. An injector device comprising the pharmaceutical composition of any one of claims 1-112.

Images