Compositions and methods for modulating complement activity

Abstract

To provide a sustained release formulation comprising an active ingredient and a release modulating matrix, the formulation being a therapeutic formulation with less burdensome administration requirements.SOLUTION: Provided is a sustained release formulation comprising: a polypeptide comprising a C5 inhibitory cyclic polypeptide having a specific amino acid sequence; and a release modulating matrix comprising a polymer, wherein the polymer comprises poly lactic-co-glycolic acid (PLGA).SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present disclosure relates to compositions and methods for modulating complement activity. [Background technology]

[0002] The vertebrate immune response is composed of adaptive and innate immune components. The adaptive immune response is selective for specific pathogens and is slow to respond, while the innate immune response components recognize a broad range of pathogens and respond rapidly to infection. One such component of the innate immune response is the complement system.

[0003] The complement system comprises approximately 20 circulating complement component proteins synthesized primarily by the liver. This particular component of the immune response was first named "complement" due to the observation that it complemented the antibody response in the destruction of bacteria. These proteins remain in an inactive form prior to activation in response to infection. Activation is initiated by pathogen recognition and occurs via a proteolytic cleavage pathway that leads to pathogen destruction. Three such pathways are known in the complement system: the classical pathway, the lectin pathway, and the alternative pathway. The classical pathway is activated when IgG or IgM molecules bind to the surface of a pathogen. The lectin pathway is initiated by mannan-binding lectin proteins recognizing sugar residues on bacterial cell walls. The alternative pathway maintains a low level of activity in the absence of any specific stimulus. Although all three pathways differ in their initiating events, they all converge on the cleavage of complement component C3, which is cleaved into two products, C3a and C3b. Of these, C3b binds covalently to pathogen surfaces, whereas C3a acts as a diffusible signal to promote inflammation and recruit circulating immune cells. Surface-bound C3b forms complexes with other components and initiates a cascade of reactions between subsequent components of the complement system. The requirement for surface attachment ensures that complement activity remains localized, minimizing destruction of non-target cells.

[0004] C3b attached to pathogens promotes pathogen destruction in two ways. In one pathway, C3b is directly recognized by phagocytes, leading to engulfment of the pathogen. In the second pathway, C3b attached to pathogens initiates the formation of the membrane attack complex (MAC). In the first step, C3b combines with other complement components to form the C5 convertase complex. Depending on the initial complement activation pathway, the components of this complex can vary. C5 convertase formed as a result of the classical complement pathway contains C4b and C2a in addition to C3b. When formed by the alternative pathway, C5 convertase contains two subunits of C3b and one Bb component.

[0005] Complement component C5 is cleaved into C5a and C5b by one of the C5 convertase complexes. C5a, like C3a, diffuses into the circulation, promoting inflammation and acting as a chemoattractant for inflammatory cells. C5b remains attached to the cell surface, where it interacts with C6, C7, C8, and C9 to form MACs. MACs are hydrophilic pores that span the membrane and facilitate the free flow of fluid into and out of cells, thereby destroying them.

[0006] A key component of overall immune activity is the immune system's ability to distinguish between self and non-self cells. Pathological conditions arise when the immune system is unable to make this distinction. In the case of the complement system, vertebrate cells express proteins that protect them from the effects of the complement cascade. This ensures that the complement system's targets are limited to pathogenic cells. Many complement-related disorders and diseases are associated with the abnormal destruction of self cells by the complement cascade. In one example, subjects suffering from paroxysmal nocturnal hemoglobinuria (PNH) are unable to synthesize functional versions of the complement regulatory proteins CD55 and CD59 on hematopoietic stem cells. This leads to complement-mediated hemolysis and various downstream complications. Experimental evidence suggests that PNH and other complement-related disorders can be alleviated through inhibition of complement activity. Summary of the Invention [Problem to be solved by the invention]

[0007] While several therapeutic complement inhibitors are available for treating patients, most require frequent administration via intravenous or subcutaneous delivery. These frequent, often daily, administrations reduce quality of life and patient compliance. There remains a need in the art for therapeutic formulations that have less burdensome administration requirements. Embodiments of the present disclosure address this by providing the related formulations and methods described herein. [Means for solving the problem]

[0008] In some embodiments, the present disclosure provides a sustained-release formulation comprising a polypeptide, wherein the polypeptide is a C5 inhibitory cyclic polypeptide comprising the amino acid sequence of SEQ ID NO: 1; and a modified-release matrix comprising a polymer, wherein the polymer comprises polylactic acid-co-glycolic acid (PLGA). The modified-release matrix may comprise particles. The particles may comprise microparticles. The PLGA may comprise a ratio of polylactic acid to polyglycolic acid of about 25:75 to about 75:25. The PLGA may comprise a ratio of polylactic acid to polyglycolic acid of about 50:50. The modified-release matrix may comprise an emulsion. The emulsion may comprise a single emulsion. The emulsion may comprise a double emulsion. The sustained-release formulation may comprise an excipient. The excipient may comprise a pore-forming excipient (PFE). The pore-forming excipient may be selected from the group consisting of medium-chain triglycerides, Pluronic® F-127, and poly(ethylene glycol) (PEG). The particles may comprise a diameter of about 5 μm to about 200 μm. The polypeptide may comprise a cyclic bond. The polypeptide may comprise a modified lysine residue. The polypeptide may comprise a lipid moiety. The polypeptide may comprise a PEG moiety. The polypeptide may comprise zilucoplan. The sustained-release formulation may comprise about 10% to about 95% by weight of a modified-release matrix. The sustained-release formulation may comprise about 50% to about 90% by weight of a modified-release matrix. The sustained-release formulation may comprise about 10% to about 50% by weight of a polypeptide. The polypeptide may be uniformly distributed in the modified-release matrix.

[0009] In some embodiments, the present disclosure provides a method for preparing a sustained-release formulation, the method comprising: preparing an organic phase solution; preparing an aqueous phase solution; and preparing an emulsion of the organic phase solution and the aqueous phase solution to prepare the sustained-release formulation, wherein the organic phase solution is prepared by mixing an organic solvent, PLGA, and a polypeptide, and the aqueous phase solution is prepared by mixing an aqueous solution with an emulsion stabilizer. The organic solvent may include dichloromethane (DCM). The aqueous solution may include phosphate-buffered saline. The emulsion stabilizer may include polyvinyl alcohol (PVA). The organic solvent may be removed from the emulsion by evaporation. The evaporation may be performed by quench evaporation. The evaporation may be performed by rotary evaporation. Particles may be formed as a result of the evaporation. The polypeptide may be uniformly distributed in the particles. The polypeptide may be mixed into the organic phase solution at a concentration sufficient to obtain about 10% to about 50% by weight of the polypeptide in the sustained-release formulation. The polypeptide may be mixed in the organic phase solution at a concentration sufficient to obtain about 36% to about 38% by weight of the polypeptide in the sustained-release formulation. The polypeptide may include zilucoplan. The sustained-release formulation may include zilucoplan-PLGA particles.

[0010] In some embodiments, the present disclosure provides a sustained-release formulation prepared according to any of the methods described herein. The sustained-release formulation may have sustained-release characteristics including a low initial burst in polypeptide release and / or the ability to obtain an effective concentration of the polypeptide in a medium in which the polypeptide is released from the sustained-release formulation. The ability to obtain an effective concentration of the polypeptide in a medium in which the polypeptide is released from the sustained-release formulation may extend over a specific period of time. The specific period of time may include about 1 week to about 3 weeks. The effective concentration may be about 4,000 ng / mL to about 12,000 ng / mL. The sustained-release characteristics may include an initial burst in polypeptide release of about 0% to about 20% of the total amount of polypeptide contained in the sustained-release formulation.

[0011] In some embodiments, the present disclosure provides a method of administering a polypeptide, comprising administering a sustained-release formulation described herein, wherein the polypeptide comprises zilucoplan. The sustained-release formulation may be administered by subcutaneous injection. The sustained-release formulation may be administered weekly or biweekly. The polypeptide may be released from the sustained-release formulation after administration. The release of the polypeptide may exhibit a burst of less than 5%. The sustained-release formulation may be administered at a dosage sufficient to administer about 2 mg / kg to about 20 mg / kg of the polypeptide. The sustained-release formulation may be administered at a dosage sufficient to administer about 100 mg to about 200 mg of zilucoplan.

[0012] In some embodiments, the present disclosure provides a method of reducing hemolysis in a subject, comprising administering a sustained release formulation described herein, wherein the sustained release formulation comprises zilucoplan.

[0013] In some embodiments, the present disclosure provides a method of treating a complement-related indication, comprising administering a sustained release formulation described herein, wherein the sustained release formulation comprises zilucoplan. The complement-related indication may include one or more of paroxysmal nocturnal hemoglobinuria, myasthenia gravis, inflammatory indications, wounds, burns, autoimmune indications, pulmonary indications, cardiovascular indications, neurological indications, renal-related indications, diabetes-related indications, ophthalmic indications, and pregnancy-related indications.

[0014] In some embodiments, the present disclosure provides a sustained release formulation comprising an active ingredient and a modified release matrix comprising a polymer, wherein the polymer comprises PLGA. The modified release matrix may comprise particles. The particles may comprise nanoparticles or microparticles. The PLGA may comprise a ratio of polylactic acid to polyglycolic acid of about 25:75 to about 75:25. The PLGA may comprise a ratio of polylactic acid to polyglycolic acid of about 50:50. The modified release matrix may comprise an emulsion. The emulsion may comprise a single emulsion. The emulsion may comprise a double emulsion. The sustained release formulation may comprise an excipient. The excipient may comprise a PFE. The PFE may be selected from the group consisting of medium-chain triglycerides, Pluronic® F-127, and PEG. The particles may have a diameter of about 5 μm to about 200 μm. The active ingredient may comprise a therapeutic agent. The active ingredient may comprise at least one unnatural amino acid. The at least one unnatural amino acid can be selected from any of those listed in Table 2 of U.S. Patent Application Publication No. 2011 / 0172126. The active ingredient can include a cyclic bond. The active ingredient can include a modified lysine residue. The active ingredient can include a lipid moiety. The active ingredient can include a PEG moiety. The active ingredient can be a peptidomimetic. The active ingredient can be a macrocycle. The active ingredient can include a C5 inhibitor. The C5 inhibitor can be selected from the group consisting of any of those listed in Table 1 or any of those listed in Table 1 of U.S. Patent Application Publication No. 2017 / 0137468. The sustained release formulation can include about 10% to about 95% by weight of the modified release matrix. The sustained release formulation can include about 50% to about 90% by weight of the modified release matrix. The sustained release formulation can include about 10% to about 50% by weight of the active ingredient. The active ingredient can be uniformly distributed in the modified release matrix.

[0015] In some embodiments, the present disclosure provides a method for preparing a sustained-release formulation described herein, the method comprising: preparing an organic phase solution; preparing an aqueous phase solution; and preparing an emulsion of the organic phase solution and the aqueous phase solution to prepare the sustained-release formulation, wherein the organic phase solution is prepared by mixing an organic solvent, PLGA, and an active ingredient, and the aqueous phase solution is prepared by mixing an aqueous solution with an emulsion stabilizer. The organic solvent may include DCM. The aqueous solution may include phosphate buffered saline. The emulsion stabilizer may include PVA. The organic solvent may be removed from the emulsion by evaporation. The evaporation may be performed by quench evaporation. The evaporation may be performed by rotary evaporation. Particles may be formed as a result of the evaporation. The active ingredient may be uniformly distributed in the particles. The active ingredient may be mixed into the organic phase solution at a concentration sufficient to obtain about 10% to about 50% by weight of the active ingredient in the sustained-release formulation. The active ingredient may be mixed in the organic phase solution at a concentration sufficient to obtain about 36% to about 38% by weight of the active ingredient in the sustained release formulation.

[0016] In some embodiments, the present disclosure provides a sustained-release formulation prepared according to any of the methods described herein. The sustained-release formulation may have sustained-release characteristics including a low initial burst in the release of the active ingredient and / or the ability to achieve an effective concentration of the active ingredient in the medium from which the active ingredient is released from the sustained-release formulation. The ability to achieve an effective concentration of the active ingredient in the medium from which the active ingredient is released from the sustained-release formulation may extend over a specific period of time. The specific period of time may include about 1 week to about 3 weeks. The effective concentration may be about 4,000 ng / mL to about 12,000 ng / mL. The sustained-release characteristics may include an initial burst in the release of about 0% to about 20% of the total amount of active ingredient contained in the sustained-release formulation.

[0017] In some embodiments, the present disclosure provides a method of administering an active ingredient, comprising administering a sustained release formulation according to any of those described herein. The sustained release formulation may be administered by subcutaneous injection. The sustained release formulation may be administered weekly or biweekly. The active ingredient may be released from the sustained release formulation after administration. The release of the active ingredient may exhibit a burst of less than 5%. The sustained release formulation may be administered at a dosage sufficient to administer about 2 mg / kg to about 20 mg / kg of the active ingredient. The sustained release formulation may be administered at a dosage sufficient to administer about 100 mg to about 200 mg of the active ingredient.

[0018] In some embodiments, the present disclosure provides methods of reducing hemolysis in a subject by administering to the subject an active ingredient according to any of the methods described herein. In some embodiments, the present disclosure provides methods of treating a complement-related indication in a subject by administering to the subject an active ingredient according to any of the methods described herein, wherein the active ingredient comprises a C5 inhibitor. The complement-related indication may include one or more of paroxysmal nocturnal hemoglobinuria, myasthenia gravis, inflammatory indications, wounds, burns, autoimmune indications, pulmonary indications, cardiovascular indications, neurological indications, renal-related indications, diabetes-related indications, ophthalmic indications, and pregnancy-related indications.

[0019] The above and other objects, features, and advantages of particular embodiments of the present disclosure will be apparent from the following description and illustrations in the accompanying drawings. [Brief explanation of the drawings]

[0020] [Figure 1] 1 is a graph of zilucoplan concentrations in rat plasma samples obtained at various time points after administration of zilucoplan-PLGA formulations. [Figure 2] 1 is a graph of zilucoplan concentrations in non-human primate plasma samples obtained at various time points after administration of a zilucoplan-PLGA formulation. [Figure 3]1 is a graph of zilucoplan concentrations in non-human primate plasma samples obtained at various time points after administration of a zilucoplan-PLGA formulation. DETAILED DESCRIPTION OF THE INVENTION

[0021] introduction Embodiments of the present disclosure relate to compounds and compositions for modulating complement activity, and related methods of use. Complement activity protects the body from foreign pathogens, but increased or uncontrolled activity can lead to self-cell destruction. The complement regulator can be a complement inhibitor, such as zilucoplan. Zilucoplan is a macrocyclic synthetic peptide that binds to complement component 5 (C5) with subnanomolar affinity and allosterically inhibits its cleavage into C5a and C5b upon activation of the classical, alternative, or lectin pathways (see, e.g., U.S. Pat. No. 10,106,579, the contents of which are incorporated herein by reference in their entirety).

[0022] In some embodiments, the present disclosure provides formulations for the sustained release of C5-inhibitory cyclic polypeptides (e.g., zilcoplan). Such formulations may include poly(D,L-lactic-co-glycolic acid) (PLGA) technology. PLGA sustained-release formulations may be used to deliver zilcoplan at desired levels over extended periods of time. PLGA may be combined with zilcoplan to produce particles containing zilcoplan and PLGA (zilcoplan-PLGA particles). Such particles may contain uniform zilcoplan distribution and provide predictable sustained-release characteristics. Such particles may be used to deliver zilcoplan over extended periods of time and at levels sufficient to treat complement-related indications, such as paroxysmal nocturnal hemoglobinuria (PNH) and generalized myasthenia gravis (gMG). Zilcoplan-PLGA particles may be used to administer low doses of zilcoplan without the need for intravenous loading, external infusion devices, tissue-degrading enzymes, or penetration enhancers.

[0023] I. Compounds and Compositions In some embodiments, the present disclosure provides compounds (e.g., cyclic polypeptides, zilcoplan, and / or their active metabolites or variants) and compositions thereof that function to regulate complement activity. Such compounds and compositions may include inhibitors that block complement activation. As used herein, "complement activity" includes activation of the complement cascade, the formation of cleavage products from complement components such as C3 or C5, the assembly of downstream complexes following a cleavage event, or any process or event associated with or resulting from the cleavage of a complement component, e.g., C3 or C5. Complement inhibitors (e.g., complement-inhibiting cyclic polypeptides, zilcoplan, and / or their active metabolites or variants) may include C5 inhibitors that block complement activation at the level of complement component C5. Such C5 inhibitors (e.g., zilcoplan and / or its active metabolites or variants) may bind to C5 and prevent its cleavage by C5 convertase into the cleavage products C5a and C5b. As used herein, "complement component C5" or "C5" is defined as a complex that is cleaved by C5 convertase into at least the cleavage products C5a and C5b. As referred to herein, a "C5 inhibitor" includes any compound (e.g., cyclic polypeptide, zilucoplan, and / or active metabolites or variants thereof) or composition thereof that inhibits the processing or cleavage of the pre-cleaved complement component C5 complex or the cleavage products of complement component C5.

[0024] In some embodiments, the present disclosure provides cyclic polypeptide compounds (e.g., zilcoplan and / or its active metabolites or variants) and compositions thereof that function to regulate complement activity. Such cyclic polypeptide compounds and compositions thereof may include inhibitors that block complement activation. Complement-inhibiting cyclic polypeptides (e.g., zilcoplan and / or its active metabolites or variants) may include C5 inhibitors that block complement activation at the level of complement component C5. Such C5 inhibitors (e.g., zilcoplan and / or its active metabolites or variants) may bind to C5 and prevent its cleavage by C5 convertase into cleavage products C5a and C5b. As used herein, "C5-inhibiting cyclic polypeptide" includes any cyclic polypeptide (e.g., zilcoplan and / or its active metabolites or variants) or compositions thereof that inhibit the processing or cleavage of the pre-cleavage complement component C5 complex or the cleavage products of complement component C5.

[0025] It is understood that inhibition of C5 cleavage suppresses the assembly and activity of the cytolytic membrane attack complex (MAC) against glycosylphosphatidylinositol (GPI)-linked protein-deficient red blood cells. In some cases, the C5 inhibitors provided herein (e.g., C5 inhibitory cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) may also bind C5b and inhibit C6 binding and the subsequent assembly of the C5b-9MAC.

[0026] In some embodiments, the C5 inhibitor polypeptide of the present disclosure can include zilcoplan. The core amino acid sequence of zilcoplan ([cyclo(1,6)]Ac-KVERFD-(N-Me)D-Tbg-Y-azaTrp-EYP-Chg-K; SEQ ID NO: 1) comprises 15 amino acids (all L-amino acids) including four unnatural amino acids [N-methyl-aspartic acid (N-Me)D), tert-butylglycine (Tbg), 7-azatryptophan (azaTrp), and cyclohexylglycine (Chg)]; a lactam bridge between K1 and D6 of the polypeptide sequence; and a C-terminal lysine residue with a modified side chain forming N-ε-(PEG24-γ-glutamic acid-N-α-hexadecanoyl)lysine residue (also referred to herein as “B28”). The C-terminal lysine side chain modification contains a polyethylene glycol (PEG) spacer (PEG24), which is attached to an L-gamma glutamic acid residue derivatized with a palmitoyl group.

[0027] The free acid form of zilucoplan is C 172 H 278 N 24 O 55 The tetrasodium form of Zilcoplan has a molecular formula of C, a molecular weight of 3562.23 Daltons (Da), and an exact mass of 3559.97 amu. 172 H 278 N 24 O 55 It has the molecular formula Na4. The chemical structure of the sodium salt form of Zilcoplan is shown in Structure I:

[0028] [ka]

[0029] Although the four sodium ions in the structure are shown associated with the designated carboxylates, they may be associated with any of the acidic groups in the molecule. Zilcoplan drug substance is typically provided as the sodium salt form and is lyophilized.

[0030] In some embodiments, the present disclosure includes variants of zircoplan. In some zircoplan variants, the C-terminal lysine side chain moiety may be altered. In some cases, the PEG24 spacer (having 24 PEG subunits) of the C-terminal lysine side chain moiety may contain fewer or additional PEG subunits. In other cases, the palmitoyl group of the C-terminal lysine side chain moiety may be replaced with another saturated or unsaturated fatty acid. In further cases, the L-gamma glutamic acid linker (between the PEG and the acyl group) of the C-terminal lysine side chain moiety may be replaced with an alternative amino acid or non-amino acid linker.

[0031] In some embodiments, the C5 inhibitor may include an active metabolite or variant of zilcoplan. The metabolite may include ω-hydroxylation of the palmitoyl tail. Such variants may be synthesized or formed by hydroxylation of the zilcoplan precursor.

[0032] In some embodiments, zircoplan variants may include modifications to the core polypeptide sequence of zircoplan that may be used in combination with one or more of the cyclic or C-terminal lysine side chain moieties characteristic of zircoplan. Such variants may have at least 50%, at least 55%, at least 65%, at least 70%, at least 80%, at least 85%, at least 90%, or at least 95% sequence identity to the core polypeptide sequence of (SEQ ID NO: 1).

[0033] In some cases, zilcoplan variants can be cyclized by forming lactam bridges between amino acids other than those used in zilcoplan. C5 inhibitor compounds may include, but are not limited to, any of those presented in Table 1. The information supporting the listed references and listed clinical trial numbers is incorporated herein by reference in its entirety.

[0034] [Table 1-1]

[0035] [Table 1-2]

[0036] Peptide-based compounds In some embodiments, the C5 inhibitors of the present disclosure are polypeptides. According to the present disclosure, any amino acid-based molecule (natural or non-natural) can be referred to as a "polypeptide," a term that encompasses "peptides," "peptidomimetics," and "proteins." "Peptides" are conventionally considered to range in size from about 4 to about 50 amino acids. Polypeptides greater than about 50 amino acids are commonly referred to as "proteins."

[0037] C5 inhibitor polypeptides can be linear or cyclic. Cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) include any polypeptide that has one or more cyclic features, such as loops and / or internal linkages, as part of its structure. In some embodiments, such cyclic polypeptides are formed when a molecule acts as a bridging moiety to link two or more regions of a polypeptide. As used herein, the term "bridging moiety" refers to one or more components of a bridge formed between two adjacent or non-adjacent amino acids, non-natural amino acids, or non-amino acids in a polypeptide. Bridging moieties can be of any size or composition. In some embodiments, bridging moieties can include one or more chemical bonds between two adjacent or non-adjacent amino acids, non-natural amino acids, non-amino acid residues, or combinations thereof. In some embodiments, such chemical bonds can be between one or more functional groups on adjacent or non-adjacent amino acids, non-natural amino acids, non-amino acid residues, or combinations thereof. Bridging moieties can include one or more of an amide bond (lactam), a disulfide bond, a thioether bond, an aromatic ring, a triazole ring, and a hydrocarbon chain. In some embodiments, the bridging moiety comprises an amide bond between an amine functional group and a carboxylate functional group present in an amino acid, non-natural amino acid, or non-amino acid residue side chain, respectively, in some embodiments, the amine or carboxylate functional group is part of the non-amino acid residue or non-natural amino acid residue.

[0038] The C5 inhibitor polypeptide (e.g., C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) can be cyclized by the carboxy terminus, the amino terminus, or any other convenient point of attachment, such as the sulfur of a cysteine (e.g., by forming a disulfide bond between two cysteine residues in the sequence) or any side chain of an amino acid residue. Additional bonds forming a cyclic loop can include, but are not limited to, maleimide, amide, ester, ether, thiol ether, hydrazone, or acetamide bonds.

[0039] In some embodiments, a C5 inhibitor polypeptide (e.g., a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) can be synthesized on a solid support (e.g., a rink amide resin) by solid phase peptide synthesis (SPPS). SPPS methods are known in the art and can be performed with orthogonal protecting groups. In some embodiments, peptides of the present disclosure can be synthesized by SPPS with Fmoc and / or Boc chemistry. The synthesized peptide can be cleaved from the solid support using standard techniques.

[0040] C5 inhibitor polypeptides (e.g., C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) can be purified by chromatography (e.g., size exclusion chromatography (SEC) and / or high performance liquid chromatography (HPLC)). HPLC can include reverse-phase HPLC (RP-HPLC). Such peptides can be lyophilized after purification. The purified peptides can be obtained as pure peptides or as peptide salts. Residual salts constituting peptide salts can include, but are not limited to, trifluoroacetic acid (TFA), acetate, and / or hydrochloride salts. In some embodiments, the peptides of the present disclosure are obtained as peptide salts. The peptide salts can be peptide salts with TFA. Residual salts can be removed from the purified peptides by known methods (e.g., by using a desalting column).

[0041] In some embodiments, C5-inhibitory cyclic polypeptides of the present disclosure (e.g., zilcoplan and / or its active metabolites or variants) are formed using a lactam moiety. Such cyclic polypeptides can be formed, for example, by synthesis on solid-support Wang resin using standard Fmoc chemistry. In some cases, Fmoc-ASP(allyl)-OH and Fmoc-LYS(alloc)-OH are incorporated into the polypeptide to serve as precursor monomers for lactam bridge formation.

[0042] A C5 inhibitor polypeptide (e.g., a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) can be a peptidomimetic. A "peptidomimetic" or "polypeptide mimetic" is a polypeptide in which the molecule contains structural elements not found in naturally occurring polypeptides (i.e., polypeptides composed only of the 20 proteinogenic amino acids). In some embodiments, a peptidomimetic is capable of replicating or mimicking the biological action of a naturally occurring peptide. A peptidomimetic can differ from a naturally occurring polypeptide in many respects, for example, by changes in the backbone structure or by the presence of non-naturally occurring amino acids. In some cases, peptidomimetics may include amino acids with side chains not found in the 20 known proteinogenic amino acids; non-polypeptide bridging moieties used to create cyclization between terminal or internal portions of the molecule; replacement of amide bond hydrogen moieties with methyl groups (N-methylation) or other alkyl groups; replacement of peptide bonds with chemical groups or bonds that are resistant to chemical or enzymatic treatment; N- and C-terminal modifications; and / or conjugation with non-peptidic extensions (such as polyethylene glycol, lipids, carbohydrates, nucleosides, nucleotides, nucleoside bases, various small molecules, or phosphate or sulfate groups).

[0043] As used herein, the term "amino acid" includes residues of natural and unnatural amino acids. The 20 naturally occurring proteinogenic amino acids are identified and referred to herein by either their single-letter or three-letter codes as follows: aspartic acid (Asp: D), isoleucine (Ile: I), threonine (Thr: T), leucine (Leu: L), serine (Ser: S), tyrosine (Tyr: Y), glutamic acid (Glu: E), phenylalanine (Phe: F), proline (Pro: P), histidine (His: H), glycine (Gly: G), lysine (Lys: K), alanine (Ala: A), arginine (Arg: R), cysteine (Cys: C), tryptophan (Trp: W), valine (Val: V), glutamine (Gln: Q), methionine (Met: M), and asparagine (Asn: N). Naturally occurring amino acids exist in their levorotatory (L) stereoisomeric form. The amino acids referred to herein are L-stereoisomers unless otherwise specified. The term "amino acid" also includes amino acids bearing conventional amino-protecting groups (e.g., acetyl or benzyloxycarbonyl) as well as natural and unnatural amino acids protected at the carboxy terminus (e.g., as (C1-C6) alkyl, phenyl, or benzyl esters or amides; or as α-methylbenzylamides). Other suitable amino and carboxy protecting groups are known to those skilled in the art (see, e.g., Greene, TW; Wutz, PGM, Protecting Groups in Organic Synthesis; 2nd ed., 1991, New York: John Wiley & Sons, Inc., and documents cited therein, the contents of each of which are incorporated herein by reference in their entirety). The polypeptides and / or polypeptide compositions of the present disclosure can also include modified amino acids.

[0044] "Unnatural" amino acids have side chains or other features not present in the 20 naturally occurring amino acids listed above, and include, but are not limited to, N-methyl amino acids, N-alkyl amino acids, alpha, alpha-substituted amino acids, beta-amino acids, alpha-hydroxy amino acids, D-amino acids, and other unnatural amino acids known in the art (e.g., Josephson et al., (2005), J. Am. Chem. Soc., 12th ed.). 7:11727-11735; Forster, AC et al. (2003), Proc. Natl. Acad. Sci. USA 100:6353-6357; Subtelny et al. (2008), J. Am. Chem. Soc. 130:6131-6136; Hartman, MCT et al. (2007), PLoS ONE 2:e972; and Hartman et al. (2006), Proc. Natl. Acad. Sci. USA 103:4356-4361). Additional unnatural amino acids useful for optimizing polypeptides and / or polypeptide compositions of the disclosure include 1,2,3,4-tetrahydroisoquinoline-1-carboxylic acid, 1-amino-2,3-hydro-1H-indene-1-carboxylic acid, homolysine, homoarginine, homoserine, 2-aminoadipic acid, 3-aminoadipic acid, beta-alanine, aminopropionic acid, 2-aminobutyric acid, 4-aminobutyric acid, 5-aminopentanoic acid, 5-aminohexanoic acid, 6-aminocaproic acid, 2-aminoheptanoic acid, 2-aminoisobutyric acid, 3-aminoisobutyric acid, 2-aminopimelic acid, desmosine, 2,3-Diaminopropionic acid, N-ethylglycine, N-ethylasparagine, homoproline, hydroxylysine, allo-hydroxylysine, 3-hydroxyproline, 4-hydroxyproline, isodesmosine, allo-isoleucine, N-methylpentylglycine, naphthylalanine, ornithine, pentylglycine, thioproline, norvaline, tert-butylglycine, phenylglycine, azatryptophan, 5-azatryptophan, 7-azatryptophan, 4-fluorophenylalanine, penicillamine, sarcosine, homocysteine, 1-aminocyclopropanecarboxylic acid, 1-aminocyclobutanecarboxylic acid, 1-aminocyclopentanecarboxylic acid, 1-aminocyclohexanecarboxylic acid, 4-aminotetrahydro-2H-pyran-4-carboxylic acid, (S)-2-amino-3-(1H-tetrazol-5-yl) Propanoic acid, cyclopentylglycine, cyclohexylglycine, cyclopropylglycine, η-ω-methyl-arginine, 4-chlorophenylalanine, 3-chlorotyrosine, 3-fluorotyrosine, 5-fluorotryptophan, 5-chlorotryptophan, citrulline, 4-chloro-homophenylalanine, homophenylalanine, 4-aminomethyl-phenylalanine, 3-aminomethyl-phenylalanine, octylglycine, norleucine, tranexamic acid, 2-aminopentanoic acid, 2-aminohexanoic acid, 2-aminoheptanoic acid, 2-aminooctanoic acid, 2-aminononanoic acid, 2-aminodecanoic acid, 2-aminoundecanoic acid, 2-aminododecanoic acid, aminovaleric acid, and 2-(2-aminoethoxy)acetic acid, pipecolic acid, 2-carboxyazetidine, hexafluoroleucine, 3-fluorovaline, 2-amino-4,4-Difluoro-3-methylbutanoic acid, 3-fluoro-isoleucine, 4-fluoroisoleucine, 5-fluoroisoleucine, 4-methyl-phenylglycine, 4-ethyl-phenylglycine, 4-isopropyl-phenylglycine, (S)-2-amino-5-azidopentanoic acid (also referred to herein as "X02"), (S)-2-aminohept-6-enoic acid (also referred to herein as "X30"), (S)-2-aminopent-4-ynoic acid (also referred to herein as "X31") (S)-2-aminopenta-4-enoic acid (also referred to herein as "X12"), (S)-2-amino-5-(3-methylguanidino)pentanoic acid, (S)-2-amino-3-(4-(aminomethyl)phenyl)propanoic acid, (S)-2-amino-3-(3-(aminomethyl)phenyl)propanoic acid, (S)-2-amino-4-(2-aminobenzo[d]oxazol-5-yl)butanoic acid, (S)-leucinol, (S)-valinol, (S)-tert -Leucinol, (R)-3-methylbutan-2-amine, (S)-2-methyl-1-phenylpropan-1-amine, and (S)-N,2-dimethyl-1-(pyridin-2-yl)propan-1-amine, (S)-2-amino-3-(oxazol-2-yl)propanoic acid, (S)-2-amino-3-(oxazol-5-yl)propanoic acid, (S)-2-amino-3-(1,3,4-oxadiazol-2-yl)propanoic acid, (S)-2-amino-3-(1,2,4 -oxadiazol-3-yl)propanoic acid, (S)-2-amino-3-(5-fluoro-1H-indazol-3-yl)propanoic acid, and (S)-2-amino-3-(1H-indazol-3-yl)propanoic acid, (S)-2-amino-3-(oxazol-2-yl)butanoic acid, (S)-2-amino-3-(oxazol-5-yl)butanoic acid, (S)-2-amino-3-(1,3,4-oxadiazol-2-yl)butanoic acid, (S)-2-amino-3-(1,2,4-oxadiazol-3-yl)butanoic acid, (S)-2-amino-3-(5-fluoro-1H-indazol-3-yl)butanoic acid, and (S)-2-amino-3-(1H-indazol-3-yl)butanoic acid, 2-(2'MeOphenyl)-2-aminoacetic acid, tetrahydro-3-isoquinolinecarboxylic acid, and stereoisomers thereof (including, but not limited to, D and L isomers).

[0045] Additional unnatural amino acids useful in optimizing polypeptides or polypeptide compositions of the present disclosure include, but are not limited to, fluorinated amino acids in which one or more carbon-bonded hydrogen atoms have been replaced with fluorine. The number of fluorine atoms can range from one to all, inclusive, of the hydrogen atoms. Examples of such amino acids include, but are not limited to, 3-fluoroproline, 3,3-difluoroproline, 4-fluoroproline, 4,4-difluoroproline, 3,4-difluroproline, 3,3,4,4-tetrafluoroproline, 4-fluorotryptophan, 5-flurotryptophan, 6-fluorotryptophan, 7-fluorotryptophan, and stereoisomers thereof.

[0046] Additional unnatural amino acids useful in optimizing the polypeptides of the present disclosure include, but are not limited to, those disubstituted at the α-carbon. These include amino acids in which the two substituents on the α-carbon are the same, such as α-aminoisobutyric acid and 2-amino-2-ethylbutanoic acid, as well as those in which the substituents are different, such as α-methylphenylglycine and α-methylproline. Additionally, the substituents on the α-carbon can together form a ring, such as 1-aminocyclopentanecarboxylic acid, 1-aminocyclobutanecarboxylic acid, 1-aminocyclohexanecarboxylic acid, 3-aminotetrahydrofuran-3-carboxylic acid, 3-aminotetrahydropyran-3-carboxylic acid, 4-aminotetrahydropyran-4-carboxylic acid, 3-aminopyrrolidine-3-carboxylic acid, 3-aminopiperidine-3-carboxylic acid, 4-aminopiperidine-4-carboxylix acid, and stereoisomers thereof.

[0047] Additional unnatural amino acids useful in optimizing polypeptides or polypeptide compositions of the disclosure include, but are not limited to, analogs of tryptophan in which the indole ring system is replaced by another 9- or 10-membered bicyclic ring system having 0, 1, 2, 3, or 4 heteroatoms independently selected from N, O, or S. Each ring system can be saturated, partially unsaturated, or fully unsaturated. The ring system can be substituted at any substitutable atom with 0, 1, 2, 3, or 4 substituents. Each substituent can be independently selected from H, F, Cl, Br, CN, COOR, CONRR', oxo, OR, and NRR'. Each R and R' can be independently selected from H, C1-C20 alkyl, or C1-C20 alkyl-O-C1-20 alkyl.

[0048] In some embodiments, analogs of tryptophan (also referred to herein as "tryptophan analogs") may be useful in optimizing the polypeptides or polypeptide compositions of the present disclosure. Tryptophan analogs may include, but are not limited to, 5-fluorotryptophan [(5-F)W], 5-methyl-O-tryptophan [(5-MeO)W], 1-methyltryptophan [(1-Me-W) or (1-Me)W], D-tryptophan (D-Trp), azatryptophan (including, but not limited to, 4-azatryptophan, 7-azatryptophan, and 5-azatryptophan), 5-chlorotryptophan, 4-fluorotryptophan, 6-fluorotryptophan, 7-fluorotryptophan, and stereoisomers thereof. Unless indicated to the contrary, the term "azatryptophan" and its abbreviation "azaTrp" herein refer to 7-azatryptophan.

[0049] Modified amino acid residues useful for optimizing the polypeptides and / or polypeptide compositions of the present disclosure include, but are not limited to, those that are chemically blocked (reversibly or irreversibly); those that are chemically modified at their N-terminal amino group or at their side chain group; those that are chemically modified in the amide backbone, e.g., N-methylated, D (unnatural amino acid) and L (natural amino acid) stereoisomers; or residues in which a side chain functional group has been chemically modified to another functional group. In some embodiments, modified amino acids include, but are not limited to, methionine sulfoxide; methionine sulfone; aspartic acid-(beta-methyl ester), a modified amino acid of aspartic acid; N-ethylglycine, a modified amino acid of glycine; alanine carboxamide; and / or alanine. Unnatural amino acids can be purchased from Sigma-Aldrich (St. Louis, MO), Bachem (Torrance, CA), or other suppliers. Unnatural amino acids can further include any of those listed in Table 2 of US Patent Application Publication No. 2011 / 0172126, the contents of which are incorporated by reference herein in their entirety.

[0050] The present disclosure contemplates variants and derivatives of the polypeptides presented herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants). These include substitutional, insertional, deletional, and covalent variants and derivatives. As used herein, the term "derivative" is used synonymously with the term "variant" and refers to a molecule that has been modified or changed in any way relative to a reference or starting molecule.

[0051] Polypeptides of the present disclosure may include any of the following components, features, or moieties, the abbreviations of which are used herein include: "Ac" and "NH" indicate acetyl and amidated termini, respectively; "Nvl" represents norvaline; "Phg" represents phenylglycine; "Tbg" represents tert-butylglycine; "Chg" represents cyclohexylglycine; "(N-Me)X" represents the N-methylated form of an amino acid indicated by the one-letter or three-letter amino acid code in place of the variable "X" written as N-methyl-X [e.g., (N-Me)D or (N-Me)Asp represent the N-methylated form of aspartic acid, i.e., N-methyl-aspartic acid; "azaTrp" represents azatryptophan; "(4-F)Phe" represents 4-fluorophenylalanine; "Tyr(OMe)" represents O-methyltyrosine, and "Aib" represents aminoisobutyric acid; "(homo)F" or "(homo)Phe" represent homophenylalanine; "(2-OMe)Phg" refers to 2-O-methylphenylglycine; "(5-F)W" refers to 5-fluorotryptophan; and "DX" represents the given refers to the D-stereoisomer of the amino acid "X" [e.g., (D-Chg) represents D-cyclohexylglycine]; "(5-MeO)W" represents 5-methyl-O-tryptophan; "HomoC" represents homocysteine; "(1-Me-W)" or "(1-Me)W" represent 1-methyltryptophan; "Nle" represents norleucine; "Tiq" represents a tetrahydroisoquinoline residue; "Asp(T)" represents (S)-2-amino-3-(1H-tetrazol-5-yl)propanoic acid; "(3-Cl-Phe)" represents 3-chlorophenylalanine. "[(N-Me-4-F)Phe]" or "(N-Me-4-F)Phe" refers to N-methyl-4-fluorophenylalanine; "(m-Cl-homo)Phe" refers to meta-chlorohomophenylalanine; "(des-amino)C" refers to 3-thiopropionic acid; "(alpha-methyl)D" refers to alpha-methyl L-aspartic acid; "2Nal" refers to 2-naphthylalanine; "(3-aminomethyl)Phe" refers to 3-aminomethyl-L-phenyalanine; "Cle" refers to cycloleucine;"Ac-pyran" refers to 4-amino-tetrahydro-pyran-4-carboxylic acid; "(Lys-C16)" refers to N-ε-palmitoyl lysine; "(Lys-C12)" refers to N-ε-lauryl lysine; "(Lys-C10)" refers to N-ε-caprylysine; "(Lys-C8)" refers to N-ε-caprylic lysine; "[xxylyl(y,z)]" refers to a xylyl bridge moiety between two thiol-containing amino acids, where x can be m, p, or o to indicate the use of meta-, para-, or ortho-dibromoxylene (respectively) to generate the bridge moiety, and the numerical identifiers y and z position the amino acid positions within the polypeptide of the amino acids participating in the cyclization; "[cyclo(y ,z)]" refers to the formation of a bond between two amino acid residues, where the numerical identifiers y and z position the positions of the residues participating in the bond; "[cyclo-olefinyl(y,z)]" refers to the formation of a bond between two amino acid residues by olefin metathesis, where the numerical identifiers y and z position the positions of the residues participating in the bond; "[cyclo-thioalkyl(y,z)]" refers to the formation of a thioether bond between two amino acid residues, where the numerical identifiers y and z position the positions of the residues participating in the bond; "[cyclo-triazolyl(y,z)]" refers to the formation of a triazole ring between two amino acid residues, where the numerical identifiers y and z position the positions of the residues participating in the bond. "B20" refers to N-ε-(PEG2-γ-glutamic acid-N-α-octadecanedioic acid) lysine [also known as (1S,28S)-1-amino-7,16,25,30-tetraoxo-9,12,18,21-tetraoxa-6,15,24,29-tetraazahexatetracontane-1,28,46-tricarboxylic acid];

[0052] B20

[0053] [ka]

[0054] "B28" refers to N-ε-(PEG24-γ-glutamic acid-N-α-hexadecanoyl)lysine. B28

[0055] [ka]

[0056] "K14" refers to N-ε-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)-3-methylbutyl-L-lysine. All other symbols refer to the standard single-letter amino acid code.

[0057] Some C5 inhibitor polypeptides of the disclosure (e.g., C5 inhibitory cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) comprise from about 5 to about 10 amino acids, from about 6 to about 12 amino acids, from about 7 to about 14 amino acids, from about 8 to about 16 amino acids, from about 10 to about 18 amino acids, from about 12 to about 24 amino acids, or from about 15 to about 30 amino acids. In some cases, a C5 inhibitor polypeptide of the disclosure (e.g., a C5 inhibitory cyclic polypeptide) comprises at least 30 amino acids.

[0058] Some C5 inhibitor polypeptides (e.g., C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) include a C-terminal lipid moiety. Such lipid moieties can include a fatty acyl group (e.g., a saturated or unsaturated fatty acyl group). In some cases, the fatty acyl group can be a palmitoyl group.

[0059] C5 inhibitor polypeptides having fatty acid acyl groups (e.g., C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) can include one or more molecular linkers linking the fatty acid to the peptide. Such molecular linkers can include amino acid residues. In some cases, L-gamma glutamic acid residues can be used as molecular linkers. In some cases, the molecular linker can include one or more polyethylene glycol (PEG) linkers. PEG linkers of the present disclosure can include about 1 to about 5, about 2 to about 10, about 4 to about 20, about 6 to about 24, about 8 to about 32, or at least 32 PEG units.

[0060] A C5 inhibitor polypeptide (e.g., a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) can have a molecular weight of about 200 g / mol to about 600 g / mol, about 500 g / mol to about 2000 g / mol, about 1000 g / mol to about 5000 g / mol, about 3000 g / mol to about 4000 g / mol, about 2500 g / mol to about 7500 g / mol, about 5000 g / mol to about 10000 g / mol, or at least 10000 g / mol.

[0061] In some embodiments, the C5 inhibitor polypeptides of the present disclosure (e.g., C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) can include any of those listed in Table 1 of U.S. Patent Application Publication No. 2017 / 0137468, the contents of which are incorporated herein by reference in their entirety.

[0062] The C5 inhibitor polypeptides of the present disclosure (e.g., C5 inhibitory cyclic polypeptides, zilcoplan, and / or their active metabolites or variants) can be developed or modified to achieve specific binding properties. Inhibitor binding can be assessed by determining the association and / or dissociation rates with a particular target. In some cases, the compound exhibits strong and rapid association with the target combined with a slow dissociation rate. In some embodiments, the C5 inhibitor polypeptides of the present disclosure (e.g., C5 inhibitory cyclic polypeptides, zilcoplan, and / or their active metabolites or variants) exhibit strong and rapid association with C5. Such inhibitors may further exhibit a slow dissociation rate from C5.

[0063] The C5 inhibitor polypeptides disclosed herein (e.g., C5 inhibitory cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) can bind to C5 complement protein at concentrations of about 0.001 nM to about 0.01 nM, about 0.005 nM to about 0.05 nM, about 0.01 nM to about 0.1 nM, about 0.05 nM to about 0.5 nM, about 0.1 nM to about 1.0 nM, about 0.5 nM to about 1.5 ... an equilibrium dissociation constant (K D ) can be bonded.

[0064] In some embodiments, a C5 inhibitor polypeptide of the present disclosure (e.g., a C5 inhibitor cyclic polypeptide, zilcoplan, and / or an active metabolite or variant thereof) blocks the formation or generation of C5a from C5. In some cases, the formation or generation of C5a is blocked following activation of the alternative pathway of complement activation. In some cases, a C5 inhibitor polypeptide of the present disclosure (e.g., a C5 inhibitor cyclic polypeptide, zilcoplan, and / or an active metabolite or variant thereof) blocks the formation of the membrane attack complex (MAC). Such inhibition of MAC formation may result from the binding of the C5 inhibitor to the C5b subunit. A C5 inhibitor polypeptide (e.g., a C5 inhibitor cyclic polypeptide, zilcoplan, and / or an active metabolite or variant thereof) that binds to the C5b subunit may prevent C6 binding, resulting in the blocking of MAC formation. In some embodiments, this inhibition of MAC formation occurs following activation of the classical pathway, the alternative pathway, or the lectin pathway.

[0065] The C5 inhibitor polypeptides of the present disclosure (e.g., C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) can be synthesized using chemical processes. In some cases, such synthesis eliminates the risks associated with manufacturing biological products in mammalian cell systems. In some cases, chemical synthesis can be simpler and more cost-effective than biological manufacturing processes.

[0066] In some embodiments, the C5 inhibitor polypeptide (e.g., C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolite or variant) composition can be a pharmaceutical composition containing at least one pharmaceutically acceptable excipient. In some embodiments, the pharmaceutically acceptable excipient can include at least one of a salt and a buffering agent. The salt can be sodium chloride. The buffering agent can be sodium phosphate. The sodium chloride can be present at a concentration of about 0.1 mM to about 1000 mM. In some cases, the sodium chloride can be present at a concentration of about 25 mM to about 100 mM. The sodium phosphate can be present at a concentration of about 0.1 mM to about 1000 mM. In some cases, the sodium phosphate is present at a concentration of about 10 mM to about 100 mM.

[0067] In some embodiments, a C5 inhibitor polypeptide (e.g., a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) composition can contain from about 0.01 mg / mL to about 4000 mg / mL of C5 inhibitor. In some cases, the C5 inhibitor polypeptide (e.g., a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) is present at a concentration of from about 1 mg / mL to about 400 mg / mL.

[0068] As described in International Publication No. 2018106859, the contents of which are incorporated herein by reference in their entirety, zilcoplan binds to C5 and inhibits its cleavage by classical complement pathway convertases. In addition, zilcoplan binds to C5b and prevents the formation of the membrane attack complex induced by non-classical cleavage of C5. The binding and inhibitory activity of zilcoplan is not affected by the presence of clinically relevant human C5 polymorphisms (including p.R885>H / C). Unlike eculizumab, the anti-C5 monoclonal antibody inhibitor zilcoplan does not bind to surface-bound C5b-9 or soluble membrane attack complex (sC5b-9).

[0069] therapeutic agent In some embodiments, the C5 inhibitors of the present disclosure (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) are therapeutic agents. As used herein, the term "therapeutic agent" refers to any substance useful for alleviating, stabilizing, ameliorating, curing, or managing any symptom, condition, disorder, or disease. Therapeutic agents can include, but are not limited to, natural products, synthetic products, combinations of natural and synthetic products, small molecules, macromolecules, nucleic acids, aptamers, proteins, and polypeptides.

[0070] formulation In some embodiments, the present disclosure provides formulations comprising a C5 inhibitor described herein (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or a therapeutic agent. A "formulation," as used herein, is a composition prepared to contain a particular component, combination of components, and / or format. Formulation components may include, but are not limited to, solid components, liquid components, and combinations thereof. The formulations of the present disclosure may be prepared to contain or deliver an active ingredient. The term "active ingredient," as used herein, refers to a substance in a composition or formulation that produces a desired effect. The active ingredient may include a therapeutic agent. In some embodiments, the formulations of the present disclosure are prepared for therapeutic agent delivery. Such formulations may be prepared to deliver a therapeutic agent to a subject upon administration of the formulation.

[0071] In some embodiments, the formulations of the present disclosure include controlled-release formulations. As used herein, a "controlled-release formulation" is a formulation that is prepared to facilitate or promote the diffusion of one or more formulation components into the surrounding environment. Some controlled-release formulations control the release of a therapeutic agent through interactions between the therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) and the surrounding formulation components. A "sustained-release formulation" is a controlled-release formulation that promotes extended diffusion of one or more formulation components. A sustained-release formulation may delay the diffusion of a therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) from the formulation into the surrounding environment.

[0072] In some embodiments, the present disclosure provides a sustained-release formulation comprising an active ingredient (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and a modified-release matrix. As used herein, the term "modified-release matrix" refers to any network of compounds, chemical bonds, or other chemical barriers that modify the diffusion of a drug. The modified-release matrix may comprise a polymer. Such a polymer may be biodegradable. The modified-release matrix may comprise particles. Such particles may include nanoparticles and / or microparticles. In some embodiments, the modified-release matrix may comprise poly(lactic acid-co-glycolic acid) (PLGA). PLGA is a polymer composed of repeating units of poly(lactic acid) (PLA) and poly(glycolic acid) (PGA) of different lengths. The PLGA may comprise a ratio of poly(lactic acid) to poly(glycolic acid) of about 25:75 to about 75:25. The ratio may be about 50:50. The modified-release matrix may comprise an emulsion. Such emulsions may comprise a single emulsion (eg, a water-in-oil emulsion) or a double emulsion (eg, an oil-in-water-in-oil emulsion).

[0073] In some embodiments, the formulations of the present disclosure comprise controlled-release formulations of C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants). Some controlled-release formulations control the release of the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) through interactions between the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and surrounding formulation components. The sustained-release formulation may slow the diffusion of the C5 inhibitory cyclic polypeptides from the formulation into the surrounding environment.

[0074] The sustained release formulation may include an excipient. In some embodiments, a pore-forming excipient (PFE) may be included. As used herein, the term "pore-forming excipient" refers to a compound or composition used to create bubbles or pockets in the sustained release formulation or the release-modifying matrix contained therein. PFEs may include, but are not limited to, medium-chain triglycerides, Pluronic® F-127, and poly(ethylene glycol) (PEG). PEG PFEs may include, but are not limited to, PEG 3400.

[0075] The modified release matrix may include particles having a variety of diameters, hi some embodiments, the particle size is from about 5 μm to about 200 μm. The active ingredient contained in the sustained-release formulation may include a therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof). Such therapeutic agents may include natural and / or unnatural amino acids. Some therapeutic agents may include a cyclic bond. Some therapeutic agents may include modified lysine residues (e.g., having a post-translational modification to the free amine of such lysine residues). Some therapeutic agents may include a lipid moiety. Some therapeutic agents may include a PEG moiety. Some therapeutic agents may include peptidomimetics. Some therapeutic agents may include a macrocycle. The term "macrocycle" herein refers to any polymer containing at least one cyclic bond. Macrocycles may include polypeptides or proteins, including those with natural and / or unnatural amino acids. In some embodiments, the sustained-release formulation includes a C5 inhibitor polypeptide (e.g., zilucoplan) comprising SEQ ID NO: 1 as the therapeutic agent. The sustained-release formulation may include about 10% to about 50% by weight of the therapeutic agent. The therapeutic agent may be uniformly distributed in the release-modifying matrix.

[0076] The active ingredient contained in the sustained-release formulation may include a C5 inhibitory cyclic polypeptide (e.g., zilcoplan and / or its active metabolites or variants), which may include natural and / or unnatural amino acids. Some C5 inhibitory cyclic polypeptides (e.g., zilcoplan and / or its active metabolites or variants) may include modified lysine residues (e.g., having a post-translational modification to the free amine of such lysine residues). Some C5 inhibitory cyclic polypeptides (e.g., zilcoplan and / or its active metabolites or variants) may include a lipid moiety. Some C5 inhibitory cyclic polypeptides (e.g., zilcoplan and / or its active metabolites or variants) may include a PEG moiety. Some C5 inhibitory cyclic polypeptides (e.g., zilcoplan and / or its active metabolites or variants) may include peptidomimetics. Some C5 inhibitory cyclic polypeptides (e.g., zilcoplan and / or its active metabolites or variants) may include a macrocycle. In some embodiments, the sustained-release formulation includes a C5 inhibitory cyclic polypeptide comprising SEQ ID NO: 1. Such a polypeptide may include zilcoplan.

[0077] The therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) may be present in the sustained release formulation at a level of about 10% to about 50% by weight. The therapeutic agent may be uniformly distributed in the modified release matrix. The sustained release formulation of the present disclosure may comprise about 10% to about 95% modified release matrix by weight. In some embodiments, the sustained release formulation of the present disclosure comprises about 50% to about 90% modified release matrix by weight.

[0078] The sustained-release formulation can contain about 10% to about 50% by weight of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant). The C5 inhibitory cyclic polypeptide can be uniformly distributed in a release-modifying matrix.

[0079] The sustained-release formulations of the present disclosure may have different release profiles of a therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants). As used herein, the term "release profile" refers to a characteristic of a formulation based on component diffusion characteristics. The release profile, or "sustained-release profile," of a sustained-release formulation may include characteristics of the active ingredient diffusion from the sustained-release formulation. Such characteristics may include, but are not limited to, the amount of active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) released over a specific period of time, the rate of active ingredient release over a specific period of time, changes in the amount or rate of active ingredient release over a specific period of time, and the total amount of active ingredient released over time. The specific period of time may be of varying length and may be characterized by different phases of active ingredient release. Such phases may include, but are not limited to, an initial burst phase, a lag phase, and a sustained-release phase. "Initial burst" refers to a period of increased compound release after placement of the sustained release formulation in a medium. "Lagation phase" refers to the period immediately following the initial burst, in which the compound level in the sustained release formulation is depleted in the initial burst release, and compound release proceeds at a much lower level. "Slow release phase" refers to the period following the initial burst and lag phase, in which compound release proceeds at a level lower than the initial burst level but higher than the lag phase level as the sustained release formulation equilibrates with the surrounding medium and supports a more steady release of the compound. The slow release phase may include a period of reduced compound release levels, in which the compound in the sustained release formulation is depleted over time. Each phase of release may vary in length of time and compound release level depending on several factors that affect compound release. Such factors may include, but are not limited to, the characteristics of the therapeutic agent (e.g., C5 inhibitor, C5 inhibitor polypeptide, C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) incorporated into the sustained release formulation, the amount of therapeutic agent contained in the sustained release formulation, the method of loading the sustained release formulation with the therapeutic agent, the method of preparing the sustained release formulation, the sustained release formulation preparation method and composition, and the characteristics of the vehicle into which the therapeutic agent is released.The sustained release formulation composition and / or preparation method for a therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) can be varied to achieve an optimal sustained release phase length and corresponding release level, all of which contribute to the overall sustained release profile of the therapeutic agent.

[0080] The sustained-release formulations of the present disclosure may have different release profiles of the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant). Each phase of release may vary in length of time and level of compound release depending on several factors that affect compound release. Such factors may include, but are not limited to, the characteristics of the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) incorporated into the sustained-release formulation, the amount of C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) included in the sustained-release formulation, the method of loading the sustained-release formulation with the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant), the method of preparing the sustained-release formulation, the methods and compositions for preparing the sustained-release formulation, and the characteristics of the medium into which the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is released. The sustained release formulation composition for a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) and / or its preparation method may be varied to achieve an optimal sustained release phase length and corresponding release level, all of which contribute to the overall sustained release characteristics of the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant).

[0081] In some embodiments, the sustained release formulation is modified to achieve sustained release characteristics characterized by one or more of a low initial burst, an ability to achieve an effective concentration of the active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) in the medium into which the active ingredient is released from the sustained release formulation, and an ability to achieve an effective concentration of the active ingredient in the medium into which the active agent is released from the sustained release formulation over a specified period of time. As used herein, the term "effective concentration" refers to the mass per unit volume of the active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) required to achieve a specified effect.

[0082] A sustained-release formulation comprising a therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) as an active ingredient may have sustained-release properties characterized by the ability to achieve an effective concentration of the active ingredient in the medium from which the active ingredient is released from the sustained-release formulation over a period of about 1 week to about 3 weeks. The effective concentration may be about 4,000 ng / mL to about 12,000 ng / mL. The medium may be a subject or a sample obtained from a subject to which such a sustained-release formulation has been administered.

[0083] Sustained-release formulations containing a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) as an active ingredient can have sustained-release properties characterized by the ability to achieve an effective concentration of the active ingredient in the medium from which the active ingredient is released from the sustained-release formulation over a period of about 1 week to about 3 weeks. The effective concentration can be about 4,000 ng / mL to about 12,000 ng / mL. The medium can be a subject or a sample obtained from a subject to which such a sustained-release formulation has been administered.

[0084] A sustained-release formulation comprising a therapeutic agent (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) as an active ingredient can have sustained-release properties characterized by a low initial burst. In some embodiments, the low initial burst is about 0% to about 20% of the total amount of the active ingredient contained in the sustained-release formulation.

[0085] A sustained-release formulation containing a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) as an active ingredient can have sustained-release properties characterized by a low initial burst. In some embodiments, the low initial burst is about 0% to about 20% of the total amount of the active ingredient contained in the sustained-release formulation.

[0086] In some embodiments, the present disclosure provides methods for preparing sustained-release formulations (e.g., sustained-release formulations comprising a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zircoplan, and / or an active metabolite or variant thereof). Such methods may include preparing an organic phase solution and an aqueous phase solution in an emulsion formulation. The organic phase solution may be prepared by dissolving PLGA in an organic solvent. In some embodiments, the active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zircoplan, and / or an active metabolite or variant thereof) is contained in the organic phase solution prepared for the sustained-release formulation. The aqueous phase solution may be prepared by mixing an aqueous solution with an emulsion stabilizer. The term "emulsion stabilizer" herein refers to any compound useful for supporting the suspension of the organic and aqueous phases in an emulsion. In some embodiments, polyvinyl alcohol (PVA) is used as an emulsion stabilizer. The organic solvent may include dichloromethane (DCM). The aqueous solution may include phosphate-buffered saline.

[0087] In some embodiments, the present disclosure provides a method for preparing a sustained-release formulation comprising a C5 inhibitory cyclic polypeptide of the present disclosure (e.g., zilucoplan and / or its active metabolite or variant). Such a method may include preparing an organic phase solution and an aqueous phase solution in an emulsion formulation. The organic phase solution may be prepared by dissolving PLGA in an organic solvent. In some embodiments, the active ingredient (e.g., zilucoplan) is contained in the organic phase solution prepared for the sustained-release formulation. The aqueous phase solution may be prepared by mixing an aqueous solution with an emulsion stabilizer. In some embodiments, polyvinyl alcohol (PVA) is used as the emulsion stabilizer. The organic solvent may include dichloromethane (DCM). The aqueous solution may include phosphate-buffered saline.

[0088] In some embodiments, the organic solvent is removed from the sustained-release formulation after emulsification. The organic solvent may be removed by evaporation. The evaporation may be performed by quench evaporation. The term "quench evaporation" as used herein refers to an evaporation process that occurs in a solution in which the formulation undergoing evaporation draws out the organic solvent. The evaporation may be performed by rotary evaporation. Rotary evaporation (rotavap) refers to an evaporation process that utilizes a vacuum pump to reduce the ambient pressure and accelerate the evaporation process. Particles may be formed as a result of evaporation, in which the remaining formulation components are condensed. The active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolite or variant) may be uniformly distributed in the particles. The active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilcoplan, and / or an active metabolite or variant thereof) may be present in the solution used to form the emulsion at a concentration sufficient to provide about 10% to about 50% by weight of the active ingredient in the resulting sustained-release formulation. The active ingredient (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilcoplan, and / or an active metabolite or variant thereof) may be present in the solution used to form the emulsion at a concentration sufficient to provide about 36% to about 38% by weight of such active ingredient in the final sustained-release formulation. Such active ingredients may include a therapeutic agent, a C5 inhibitor, and / or a C5 inhibitor polypeptide. The C5 inhibitor polypeptide may include SEQ ID NO: 1 (e.g., zilcoplan and / or an active metabolite or variant thereof). The sustained-release formulation may include zilcoplan-PLGA particles. The C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) can be uniformly distributed throughout the particles. The C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) can be present in the solution used to form the emulsion at a concentration sufficient to provide about 10% to about 50% by weight of the C5 inhibitory cyclic polypeptide in the resulting sustained-release formulation.The C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) can be included in the solution used to form the emulsion at a concentration sufficient to achieve about 36% to about 38% by weight of such C5 inhibitory cyclic polypeptide in the final sustained-release formulation. Such a C5 inhibitory cyclic polypeptide can include SEQ ID NO: 1. The C5 inhibitory cyclic polypeptide can include zilucoplan.

[0089] For the treatment of human subjects, the compounds and compositions of the present disclosure can be formulated as pharmaceutical compositions. Such pharmaceutical compositions can include any of the sustained-release formulations described herein. Depending on the subject being treated, the mode of administration, and the type of treatment desired (e.g., prevention, prophylaxis, or therapy), pharmaceutical compositions can be formulated in a manner consistent with these parameters. Compilations of such techniques can be found in Remington: The Science and Practice of Pharmacy, 21st Edition, Lippincott Williams & Wilkins, (2005); and Encyclopedia of Pharmaceutical Technology, edited by J. Swarbrick and JC Boylan, 1988-1999, Marcel Dekker, New York, each of which is incorporated herein by reference.

[0090] isotopic variants The compounds of the present disclosure (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) may contain one or more atoms that are isotopes. As used herein, the term "isotope" refers to a chemical element that has one or more additional neutrons. In some embodiments, the compounds of the present disclosure or components of their formulations may be deuterated. As used herein, the term "deuterated" refers to a substance in which one or more hydrogen atoms have been replaced with a deuterium isotope. A deuterium isotope is an isotope of hydrogen. A hydrogen nucleus contains one proton, while a deuterium nucleus contains both a proton and a neutron. The compounds and compositions of the present disclosure may be deuterated to alter physical properties such as stability or to enable use in diagnostic and experimental applications.

[0091] The C5 inhibitory cyclic polypeptides of the present disclosure (e.g., zilucoplan and / or its active metabolites or variants) may contain one or more atoms that are isotopes. In some embodiments, the C5 inhibitory cyclic polypeptides of the present disclosure (e.g., zilucoplan and / or its active metabolites or variants) or components of formulations thereof may be deuterated. The C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be deuterated to alter physical properties such as stability or to enable use in diagnostic and experimental applications.

[0092] II. Method In some embodiments, the present disclosure provides methods related to preparing, using, and evaluating the compounds described herein (e.g., therapeutic agents, C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and compositions thereof. Such methods may include methods of using the disclosed compounds and compositions thereof for therapeutic applications. The term "therapeutic application" as used herein refers to any activity performed to alleviate, stabilize, ameliorate, cure, or address any symptom, condition, disorder, or disease. Therapeutic applications may include modulating complement activity using the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof.

[0093] In some embodiments, the present disclosure provides methods related to preparing, using, and evaluating the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions described herein. Such methods may include using the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure in therapeutic applications. Therapeutic applications may include using the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and / or compositions described herein to modulate complement activity.

[0094] Treatment indications In some embodiments, the methods of the present disclosure include methods of treating a therapeutic indication using a compound described herein (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or a composition thereof. As used herein, the term "therapeutic indication" refers to any symptom, condition, disorder, or disease that can be alleviated, stabilized, ameliorated, cured, or otherwise addressed by some form of therapy or other therapeutic intervention (e.g., administration of a complement inhibitor). Therapeutic indications may include, but are not limited to, inflammatory indications, wounds, injuries, autoimmune indications, vascular indications, neurological indications, renal-related indications, ophthalmic indications, cardiovascular indications, pulmonary indications, and pregnancy-related indications. Therapeutic indications associated with complement activity and / or dysfunction are referred to herein as "complement-related indications." In some embodiments, the methods of the present disclosure may include treating a complement-related indication by administering a complement inhibitor compound described herein and / or a composition thereof. Administration may include use of sustained release formulations described herein, including those formulated for sustained release of zilucoplan.

[0095] In some embodiments, the methods of the present disclosure include methods of treating a therapeutic indication using a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) and / or composition disclosed herein. The therapeutic indication may include, but is not limited to, inflammatory indications, wounds, injuries, autoimmune indications, vascular indications, neurological indications, renal-related indications, ophthalmic indications, cardiovascular indications, pulmonary indications, and pregnancy-related indications. In some embodiments, the methods of the present disclosure may include treating a complement-related indication by administering a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) and / or composition thereof (e.g., a complement inhibitor compound) disclosed herein.

[0096] In some embodiments, where complement activation contributes to the progression of a disease, disorder, and / or condition, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be useful in treating complement-related indications. Such complement-related indications may include, but are not limited to, inflammatory indications, wounds, injuries, autoimmune indications, vascular indications, neurological indications, renal-related indications, ophthalmic indications, cardiovascular indications, pulmonary indications, and pregnancy-related indications. Complement-related indications may include, but are not limited to, any of those listed in U.S. Pat. No. 10,106,579, the contents of which are incorporated herein by reference in their entirety.

[0097] In some embodiments, where complement activation contributes to the progression of a disease, disorder, and / or condition, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) may be useful in treating complement-related indications. Such complement-related indications may include, but are not limited to, inflammatory indications, wounds, injuries, autoimmune indications, vascular indications, neurological indications, renal-related indications, ophthalmic indications, cardiovascular indications, pulmonary indications, and pregnancy-related indications. Complement-related indications may include, but are not limited to, any of those listed in U.S. Pat. No. 10,106,579, the contents of which are incorporated herein by reference in their entirety.

[0098] The complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof may be useful in treating infections, disorders, and / or conditions, for example, in a subject having an infection. In some embodiments, a subject having an infection or at risk of developing sepsis or septic syndrome can be treated with a complement inhibitor described herein. In some cases, the complement inhibitor compounds can be used in the treatment of sepsis.

[0099] C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolite or variant) and compositions thereof may be useful in treating infections, disorders, and / or conditions, for example, in subjects with an infection. In some embodiments, subjects with an infection or at risk of developing sepsis or septic syndrome may be treated with a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) described herein. In some cases, a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) may be used in the treatment of sepsis.

[0100] The complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof can also be administered to improve the outcome of clinical diagnoses where complement inhibition is desired. Such diagnoses can include, but are not limited to, grafting, transplantation, implants, catheterization, intubation, and the like. In some embodiments, the complement inhibitor compounds and compositions are used to coat devices, materials, and / or biomaterials used in such diagnoses. In some embodiments, the interior surface of tubing can be coated with the compounds and compositions to prevent complement activation in bodily fluids passing through the tubing, either in vivo or ex vivo, e.g., in extracorporeal shunts, e.g., dialysis, and cardiac bypass surgery.

[0101] C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof may also be administered to improve the outcome of clinical diagnoses when complement inhibition is desired. Such diagnoses may include, but are not limited to, grafting, transplantation, implants, catheterization, intubation, and the like. In some embodiments, C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof are used to coat devices, materials, and / or biomaterials used in such diagnoses. In some embodiments, the interior surface of tubing may be coated with C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof to prevent complement activation in bodily fluids passing through the tubing, either in vivo or ex vivo, e.g., in extracorporeal shunts, e.g., dialysis, and cardiac bypass surgery.

[0102] The terms "treat," "treatment," and the like, as used herein, refer to relief from or alleviation of a pathological process. In the context of this disclosure, as it relates to any of the other conditions listed herein below, the terms "treat," "treatment," and the like, mean reducing or alleviating at least one symptom associated with such condition, or slowing or reversing the progression or expected progression of such condition.

[0103] "Lowering" or "reducing" in the context of a disease marker or symptom means a significant, often statistically significant, decrease in such levels, which can be, for example, at least 10%, at least 20%, at least 30%, at least 40% or more, preferably to levels recognized as within the normal range for individuals without such disorder.

[0104] "Increase" or "elevate" in the context of a disease marker or symptom means a significant, often statistically significant, increase in such level, which can be, for example, at least 10%, at least 20%, at least 30%, at least 40% or more, preferably to a level recognized as within the normal range for individuals without such disorder.

[0105] Efficacy of disease treatment or amelioration can be assessed, for example, by measuring disease progression, disease remission, symptom severity, pain reduction, quality of life, dosage required to maintain therapeutic efficacy, levels of disease markers, or any other measurable parameter appropriate for the given disease being treated or targeted for prevention. Monitoring the effectiveness of treatment or prevention by measuring any one or any combination of such parameters is well within the capabilities of one of ordinary skill in the art. In the context of administration of a polypeptide or pharmaceutical composition thereof, "effective against" a disease or disorder indicates that administration in a clinically relevant manner results in a beneficial effect in at least some patients, such as improvement of symptoms, cure, reduction in disease burden, reduction in tumor mass or cell count, prolongation of survival, improved quality of life, reduced need for blood transfusions, or other effect generally recognized as positive by physicians skilled in treating a particular type of disease or disorder.

[0106] A therapeutic or prophylactic effect is evidenced by a significant, often statistically significant, improvement in one or more parameters of the disease state, or by a failure to worsen or develop symptoms that would otherwise be expected. By way of example, a favorable change of at least 10%, and preferably at least 20%, 30%, 40%, 50% or more, in a measurable parameter of the disease may indicate effective treatment. The efficacy of a given compound or composition may also be determined using an experimental animal model of a given disease, as is known in the art. When an experimental animal model is used, the efficacy of the treatment is demonstrated when a statistically significant modulation of a marker or symptom is observed.

[0107] The compounds of the present disclosure can be administered in combination with additional therapeutic agents. Such combinations can be in the same composition, or the additional therapeutic agents can be administered as part of a separate composition or by another method described herein.

[0108] Paroxysmal nocturnal hemoglobinuria (PNH) Complement-related indications can include paroxysmal nocturnal hemoglobinuria (PNH). In some embodiments, complement inhibitor compounds and compositions can be used to treat, prevent, or delay the onset of PNH. In some embodiments, treatment can involve preventing hemolysis of PNH red blood cells in a dose-dependent manner.

[0109] Acquired mutations in the phosphatidylinositol glycan anchor biosynthesis, class A (PIG-A) gene, derived from pluripotent hematopoietic stem cells, result in a rare disorder known as paroxysmal nocturnal hemoglobinuria (PNH) (Pu, JJ et al., "Paroxysmal nocturnal hemoglobinuria from bench to bedside," Clin Transl Sci., June 2011, Vol. 4(3), pp. 219-24). PNH is characterized by bone marrow failure, hemolytic anemia, and thrombosis. The PIG-A gene product is required for the production of the glycolipid anchor, glycosylphosphatidylinositol (GPI), which is used to anchor proteins to the plasma membrane. Two complement regulatory proteins, CD55 and CD59, become nonfunctional in the absence of GPI, leading to complement-mediated destruction of these cells. Complement inhibitors are particularly useful in the treatment of PNH. In some embodiments, compounds and compositions can be used to treat, prevent, or delay the onset of paroxysmal nocturnal hemoglobinuria (PNH) or complement-associated anemia. Subjects with PNH are unable to synthesize functional versions of the complement regulatory proteins CD55 and CD59 on hematopoietic stem cells. This leads to complement-mediated hemolysis and various downstream complications. As used herein, the term "downstream" or "downstream complications" refers to any event that occurs after and as a result of another event. In some cases, downstream events are events that occur after and as a result of C5 cleavage and / or complement activation.

[0110] PNH is characterized by low hemoglobin, increased levels of lactate dehydrogenase and bilirubin, and decreased levels of haptoglobin. Symptoms of PNH include symptoms of anemia, such as fatigue, headache, shortness of breath, chest pain, dizziness, and lightheadedness.

[0111] Current treatments for PNH include the use of eculizumab (Alexion Pharmaceuticals, Cheshire, Connecticut). In some cases, eculizumab may be ineffective due to mutations in C5, a short half-life, immune responses, or other reasons. In some embodiments, the methods of the present disclosure include methods of treating a subject with PNH, where such subject has previously been treated with eculizumab. In some cases, eculizumab is ineffective in such subjects, making treatment with a compound of the present disclosure important for therapeutic relief. In some embodiments, the compounds of the present disclosure can be used to treat subjects who are resistant to eculizumab treatment. Such subjects may include subjects with the R885H / C polymorphism, which confers resistance to eculizumab. In some cases, the compounds of the present disclosure are administered simultaneously or in conjunction with eculizumab therapy. In such cases, the subject may experience one or more beneficial effects of such combination therapy, including, but not limited to, more effective relief, more rapid relief, and / or fewer side effects.

[0112] Inflammatory indications Therapeutic indications that may be addressed with the compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may include inflammatory indications. As used herein, the term "inflammatory indication" refers to therapeutic indications involving immune system activation. Inflammatory indications may include complement-related indications. Inflammation may be upregulated during the proteolytic cascade of the complement system. While inflammation may have beneficial effects, excessive inflammation may lead to various pathologies (Markiewski et al., 2007, Am J Pathol. 17:715-727). In some embodiments, the complement inhibitor compounds and compositions of the present disclosure may be used to treat, prevent, or delay the onset of inflammatory indications.

[0113] Inflammatory indications include acute disseminated encephalomyelitis (ADEM), acute necrotizing hemorrhagic leukoencephalitis, Addison's disease, agammaglobulinemia, alopecia areata, amyloidosis, ankylosing spondylitis, acute antibody-mediated rejection after organ transplantation, anti-GBM / anti-TBM nephritis, antiphospholipid syndrome (APS), autoimmune angioedema, autoimmune aplastic anemia, autoimmune autonomic neuropathy, autoimmune hepatitis, autoimmune hyperlipidemia, autoimmune immunodeficiency, autoimmune inner ear disease (AIED), autoimmune myocarditis, autoimmune pancreatitis, autoimmune retinopathy, autoimmune thrombocytopenic purpura (ATP), autoimmune thyroid disease, autoimmune urticaria, axonal and neuronal neuropathy, bacterial sepsis and septic shock, and Balo's disease. disease), Behçet's disease, bullous pemphigoid, cardiomyopathy, Castleman's disease, celiac disease, Chagas disease, chronic fatigue syndrome, chronic inflammatory demyelinating polyneuropathy (CIDP), chronic recurrent multifocal osteomyelitis (CRMO), Churg-Strauss syndrome, cicatricial pemphigoid / benign mucous membrane pemphigoid, Crohn's disease, Cogan's syndromesyndrome), cold agglutinin disease, congenital heart block, Coxsackie myocarditis, Crest disease, essential mixed cryoglobulinemia, demyelinating neuropathy, dermatitis herpetiformis, dermatomyositis, Devic's disease (neuromyelitis optica), type 1 diabetes, discoid lupus, Dressler's syndrome, endometriosis, eosinophilic esophagitis, eosinophilic fasciitis, erythema nodosum, experimental allergic encephalomyelitis, Evans' syndrome, fibromyalgia, fibrosing alveolitis, giant cell arteritis (lateral) arteritis), glomerulonephritis, Good Pasteur's disease, granulomatosis with polyangiitis (GPA) (see Wegener's granulomatosis), Graves' disease, Guillain-Barré syndrome, Hashimoto's encephalitis, Hashimoto's thyroiditis, hemolytic anemia (atypical hemolytic uremic syndrome and plasma therapy-resistant atypical hemolytic uremic syndrome), Henoch-Schönlein purpura, herpes gestationis, hypogammaglobulinemia, idiopathic thrombocytopenic purpura (ITP), IgA nephropathy, IgG4-related sclerosing disease, immune deficiency Nodular lipoprotein, inclusion body myositis, insulin-dependent diabetes mellitus (type 1), interstitial cystitis, juvenile arthritis, juvenile diabetes mellitus, Kawasaki syndrome, Lambert-Eaton syndrome, large-vessel vasculopathy, leukocytoclastic vasculitis, lichen planus, lichen sclerosus, lignified conjunctivitis, linear immunoglobulin A disease (LAD), lupus (SLE), Lyme disease, Meniere's disease, microscopic polyangiitis, mixed connective tissue disease (MCTD), Mooren's ulcer, Mucha-Habermann disease, multiple endocrine neoplasia syndrome, multiple sclerosis, multifocal motor neuropathy, myositis, myasthenia gravis, narcolepsy, neuromyelitis optica (Devic's disease), neutropenia, ocular cicatricial pemphigoid, optic neuritis, osteoarthritis, relapsing rheumatoid arthritis, PANDAS (pediatric autoimmune neuropsychiatric disorders associated with streptococcal disease), paraneoplastic cerebellar degeneration, paroxysmal nocturnal hemoglobinuria (PNH), Parry-Romberg syndrome, Parsonage-Turner syndromesyndrome), pars planitis (peripheral uveitis), pemphigus, peripheral neuropathy, perivenous encephalomyelitis, pernicious anemia, POEMS syndrome, polyarteritis nodosa, autoimmune polyglandular syndrome types I, II, and III, polyendocrine deficiency, polymyalgia rheumatica, polymyositis, post-myocardial infarction syndrome, post-pericardiotomy syndrome, progesterone dermatitis, primary biliary cirrhosis, primary sclerosing cholangitis, psoriasis, psoriatic arthritis, idiopathic pulmonary fibrosis , pyoderma gangrenosum, pure red cell aplasia, Raynaud's phenomenon, reactive arthritis, reflex sympathetic dystrophy, Reiter's syndrome, relapsing polychondritis, restless legs syndrome, retroperitoneal fibrosis, rheumatic fever, rheumatoid arthritis, sarcoidosis, Schmidt's syndrome, scleritis, scleroderma, Shiga toxin-producing Escherichia coli hemolytic uremic syndrome (STEC-HUS), Sjögren's syndrome, small vessel vasculopathy, sperm-testicular autoimmunity (Sperm & testicular autoimmunity), stiff-person syndrome, subacute bacterial endocarditis (SBE), Susac syndrome, sympathetic ophthalmia, Takayasu's arteritis, temporal arteritis / giant cell arteritis, thrombocytopenic purpura (TTP), Tolosa-Hunt syndrome, transverse myelitis, tubular autoimmune disorder, ulcerative colitis, undifferentiated connective tissue disease (UCTD), uveitis, vesicular-bullous dermatosis, vasculitis, vitiligo, and Wegener's granulomatosis (also known as granulomatosis with polyangiitis (GPA)).

[0114] sterile inflammation Inflammatory indications may include sterile inflammation. Sterile inflammation is inflammation that occurs in response to stimuli other than infection. Sterile inflammation may be a general response to stress, such as genomic stress, hypoxic stress, nutrient stress, or endoplasmic reticulum stress, caused by physical, chemical, or metabolic noxious stimuli. Sterile inflammation may contribute to the pathogenesis of many diseases, including, but not limited to, ischemia-induced injury, rheumatoid arthritis, acute lung injury, drug-induced liver injury, inflammatory bowel disease, and / or other diseases, disorders, or conditions. Methods and compounds for treating, preventing, and / or delaying the mechanisms and symptoms of sterile inflammation may include any of those taught in Rubartelli et al., Frontiers in Immunology, 2013, Vol. 4, pp. 398-399; Rock et al., Annu Rev Immunol., 2010, Vol. 28, pp. 321-342; or U.S. Patent No. 8,101,586, the contents of each of which are incorporated herein by reference in their entireties. In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitor, C5 inhibitor polypeptide, C5 inhibitor cyclic polypeptide, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof described herein may be used to treat, prevent, or delay the onset of sterile inflammation. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of sterile inflammation.

[0115] Systemic Inflammatory Response (SIRS) and Sepsis Inflammatory indications can include systemic inflammatory response syndrome (SIRS). SIRS is inflammation that affects the entire body. When SIRS is caused by infection, it is called sepsis. SIRS can also be caused by non-infectious events such as trauma, injury, burns, ischemia, hemorrhage, and / or other conditions. During sepsis and SIRS, complement activation leads to excessive production of complement activation products, which can cause multiple organ failure (MOF) in a subject. In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein can be used to treat and / or prevent SIRS. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure can be used to treat and / or prevent SIRS. Complement inhibitor compounds and compositions can be used to regulate and / or balance complement activation for the prevention and treatment of SIRS, sepsis, and / or MOF. C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions can be used to regulate and / or balance complement activation for the prevention and treatment of SIRS, sepsis, and / or MOF. Methods for administering complement inhibitors to treat SIRS and sepsis can include those taught in Rittirsch et al., Clin Dev Immunol, 2012, p. 962927; U.S. Patent Application Publication No. 2013 / 0053302; or U.S. Patent No. 8,329,169, the contents of each of which are incorporated herein by reference in their entireties.

[0116] Acute respiratory distress syndrome (ARDS) Inflammatory indications may include acute respiratory distress syndrome (ARDS). ARDS is widespread inflammation of the lungs and can be caused by trauma, infection (e.g., sepsis), severe pneumonia, and / or inhalation of harmful substances. ARDS is typically a severe, life-threatening complication. Studies suggest that neutrophils may contribute to the development of ARDS by influencing the accumulation of polymorphonuclear cells in damaged alveoli and interstitial tissues of the lung. In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan and / or their active metabolites or variants) and / or compositions described herein may be used to treat and / or prevent the development of ARDS. The complement inhibitor compounds and compositions may be administered to reduce and / or prevent tissue factor production in alveolar neutrophils. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions disclosed herein may be used to treat and / or prevent the development of ARDS. C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof can be administered to reduce and / or prevent tissue factor production in alveolar neutrophils. Complement inhibitor compounds and compositions thereof can further be used to treat, prevent, and / or delay ARDS, optionally according to any of the methods taught in WO 2009 / 014633, the contents of which are incorporated herein by reference in their entirety. C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof can further be used to treat, prevent, and / or delay ARDS, optionally according to any of the methods taught in WO 2009 / 014633, the contents of which are incorporated herein by reference in their entirety.

[0117] periodontitis Inflammatory indications may include periodontitis. Periodontitis is a widespread chronic inflammation that causes destruction of periodontal tissues, the tissues that support and surround the teeth. The condition also includes alveolar bone loss (the bone that holds the teeth). Periodontitis may be caused by poor oral hygiene, which leads to bacterial buildup at the gum line, also known as plaque. Certain health conditions, such as diabetes or malnutrition and / or habits such as smoking, may increase the risk of periodontitis. Periodontitis may increase the risk of stroke, myocardial infarction, atherosclerosis, diabetes, osteoporosis, preterm labor, and other health problems. Studies have shown a correlation between periodontitis and local complement activity. Periodontal bacteria may inhibit or activate certain components of the complement cascade. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat or prevent the development of periodontitis and / or related conditions. In some embodiments, the C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat or prevent the development of periodontitis and / or related conditions. Complement activation inhibitors and methods of treatment may include any of those taught in Hajishengallis, Biochem Pharmacol., 2010, 15th Edition, Vol. 80(12), p. 1, and Lambris, or U.S. Patent Application Publication No. 2013 / 0344082, the contents of each of which are incorporated herein by reference in their entireties.

[0118] dermatomyositis Inflammatory indications can include dermatomyositis. Dermatomyositis is an inflammatory muscle disease characterized by muscle weakness and chronic myositis. Dermatomyositis often begins with an accompanying skin rash or precedes muscle weakness. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can be used to treat, prevent, or delay the onset of dermatomyositis. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure can be used to treat, prevent, or delay the onset of dermatomyositis.

[0119] Rheumatoid arthritis Inflammatory indications can include rheumatoid arthritis, an autoimmune condition that affects the wrists and small joints of the hands. Typical symptoms include pain, stiffness, swelling, and a sense of heat. Activated components of the complement system contribute to the development of rheumatoid arthritis when products of the complement cascade mediate proinflammatory activities, such as vascular permeability and tone, leukocyte chemotaxis, and activation and lysis of multiple cell types (see Wang et al., Proc. Natl. Acad. Sci., 1995, 92, 8955-8959). Wang et al. demonstrated that inhibition of the C5 complement cascade in animals prevents the onset of arthritis and ameliorates established disease. Complement activation inhibitors and methods of treatment may include any of those taught in Wang et al., Proc. Natl. Acad. Sci., 1995, 92:8955-8959, the contents of which are incorporated herein by reference in their entirety. In some embodiments, complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions described herein may be used to treat or prevent the development of rheumatoid arthritis. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or active metabolites or variants thereof) and compositions of the present disclosure may be used to treat or prevent the development of rheumatoid arthritis.

[0120] asthma Inflammatory indications may include asthma. Asthma is a chronic inflammation of the bronchi, the airways that allow air to pass into and out of the lungs. The condition is characterized by bronchial narrowing, inflammation, and hyperresponsiveness. Typical symptoms include periods of wheezing, chest tightness, coughing, and shortness of breath. Asthma is the most common respiratory disorder. Complement proteins C3 and C5 are associated with many pathophysiological features of asthma, such as inflammatory cell infiltration, mucus secretion, enhanced vascular permeability, and smooth muscle cell contraction. Therefore, it has been suggested that downregulation of complement activation may be used to treat, manage, or prevent asthma. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of asthma. In some embodiments, the C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure can be used to treat, prevent, or delay the onset of asthma. Complement activation inhibitors and treatment methods can include any of those taught in Khan et al., Respiratory Med., April 2014, Vol. 108(4), pp. 543-549, the contents of which are incorporated herein by reference in their entirety.

[0121] anaphylaxis Inflammatory indications can include anaphylaxis. Anaphylaxis is a severe, potentially life-threatening allergic reaction. Anaphylaxis can cause shock, characterized by, for example, a sudden drop in blood pressure, narrowing of the airways, difficulty breathing, a rapid pulse, a rash, nausea, and vomiting. Cardiopulmonary collapse during anaphylaxis is associated with complement activation and the production of C3a and C5a anaphylatoxins. Balzo et al. reported animal studies showing that complement activation significantly enhances cardiac dysfunction during anaphylaxis (Balzo et al., Circ Res., September 1989, Vol. 65(3):847-57). Complement activation inhibitors and treatment methods can include any of those taught in Balzo et al., the contents of which are incorporated herein by reference in their entirety. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of anaphylaxis. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of anaphylaxis.

[0122] intestinal inflammation Inflammatory indications may include inflammatory bowel disease (IBD). IBD is a relapsing condition with periods of mild to severe inflammation or periods of remission. Common symptoms include diarrhea, fatigue and fever, abdominal pain, weight loss, loss of appetite, and bloody stools. Types of IBD include ulcerative proctitis, dextran sulfate sodium colitis, proctosigmoitidis, left-sided colitis, panconitis, and severe acute ulcerative colitis. IBD, such as dextran sulfate sodium colitis and ulcerative colitis, has been associated with complement activation (Webb et al., Int J Med Pharm Case Reports, 2015, Vol. 4(5), pp. 105-112; and Aomatsu et al., J Clin Biochem Nutr., 2013, Vol. 52(1), pp. 72-75). Complement activation inhibitors and treatment methods can include any of those taught in Webb et al. or Aomatsu et al., the contents of each of which are incorporated herein by reference in their entireties. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of IBD. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of IBD.

[0123] Systemic inflammation during cardiopulmonary bypass Inflammatory indications may include inflammatory responses induced by cardiopulmonary bypass (CBP). CBP is a technique used during surgery to replace the functions of the heart and lungs and maintain blood circulation and blood oxygenation. CBP induces a systemic inflammatory response that can lead to complications in surgical patients. The suggested cause may be due to activation of blood in contact with artificial surfaces during extracorporeal circulation. The inflammatory response can lead to SIRS, which can be life-threatening.

[0124] Complement activation is associated with the inflammatory response induced by CBP. Studies suggest that the terminal components C5a and C5b-9 directly contribute to platelet and neutrophil activation during extracorporeal blood circulation, and C5 has been identified as a therapeutic moiety for the prevention and treatment of the inflammatory response induced by CBP (Rinder et al., J Clin Invest., 1995, 96(3), pp. 1564-1572). Complement activation inhibitors and therapeutic methods may include any of those taught in Rinder et al., J Clin Invest., 1995, 96(3), pp. 1564-1572, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof may be used to treat, prevent, or delay the onset of an inflammatory response induced by CBP. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or active metabolites or variants thereof) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of an inflammatory response induced by CBP.

[0125] Organ or tissue transplant rejection Inflammatory indications can include immune rejection of a transplant. The transplant can be an organ (e.g., heart, kidney, liver, lung, intestine, thymus, and pancreas) or tissue (e.g., bone, tendon, skin, cornea, vein). Various types of transplants include autografts (transplantation of a patient's own tissue), allografts (transplantation between two members of the same species), or xenografts (transplantation between members of different species, e.g., animal to human). Complications after organ transplantation occur when the recipient's immune system attacks the transplanted tissue. Rejection can be hyperacute, referring to a reaction occurring within minutes of transplantation, typically occurring when the antigen is non-compatible. Acute rejection occurs within a week or several months after transplantation. Some rejections are chronic and occur over many years.

[0126] Graft rejection and associated inflammation are linked to the complement system. The complement cascade is involved in transplantation in several ways, including as an effector mechanism for antibody-mediated allograft injury; promoting ischemia-reperfusion injury; and alloantibody formation and function (Sheen and Heeger, Curr Opin Organ Transplant. 2015, 20(4), pp. 468-75). Complement-targeted therapies have been shown to have significant benefits for the survival and health of transplant recipients. For example, studies have shown that C5 inhibition with eculizumab reduces the incidence of early antibody-mediated rejection (AMR) of organ allografts (Stegall et al., Nature Reviews Nephrology 8(11):670-678, 2012), and that C5 inhibition can prevent acute cardiac tissue damage in an ex vivo model of pig-to-human xenotransplantation (Kroshus et al., Transplantation 15(60):1194-202, 1995). Complement activation inhibitors and methods of treatment may include any of those taught in Stegall et al., Nature Reviews Nephrology, Vol. 8 (Issue 11), pp. 670-678, 2012; Kroshus et al., Transplantation, 1995, 15th Edition, Vol. 60 (Issue 11): pp. 1194-202; and Sheen and Heeger, Curr Opin Organ Transplant., 2015, Vol. 20 (Issue 4), pp. 468-475, the contents of each of which are incorporated herein by reference in their entireties.In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof may be used to treat a subject having or receiving a transplanted organ or tissue. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or active metabolites or variants thereof) and / or compositions of the present disclosure may be used to treat a subject having or receiving a transplanted organ or tissue.

[0127] wounds and injuries Therapeutic indications that may be addressed with the compounds and / or compositions of the present disclosure may include wounds and injuries. The term "injury" herein typically refers to physical trauma but may also include localized infection or disease processes. Injuries may be characterized by harm, damage, or destruction caused by an external event affecting a body part and / or organ. Non-limiting examples of injuries include head trauma and crush injuries. Wounds are associated with cuts, blows, burns, and / or other impacts on the skin, leaving the skin in a broken or damaged state. Wounds and injuries may include complement-related indications. Wounds and injuries are acute but, if not treated appropriately, can lead to chronic complications and / or inflammation. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat and / or promote healing of different types of wounds and / or injuries. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat and / or promote healing of different types of wounds and / or injuries.

[0128] wounds and burns In some embodiments, the disclosed complement inhibitor compounds and compositions can be used to treat and / or promote wound healing. Healthy skin provides a waterproof, protective barrier against pathogens and other environmental effectors. Skin also regulates body temperature and fluid evaporation. When skin is wounded, these functions are disrupted, making skin healing difficult. Wounds initiate a series of physiological processes involving the immune system to repair and regenerate tissue. Complement activation is one of these processes. As taught in van de Goot et al., J Burn Care Res, 2009, Vol. 30, pp. 274-280, and Cazander et al., Clin Dev Immunol, 2012, 2012:534-291, the contents of each of which are incorporated herein by reference in their entireties, complement activation studies have identified several complement components involved in wound healing. In some cases, complement activation can be excessive, causing cell death and increased inflammation (leading to impaired wound healing and chronic wounds). In some cases, complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can be used to reduce or eliminate such complement activation and promote wound healing. Treatment with complement inhibitor compounds and compositions may be carried out according to any of the methods for treating wounds disclosed in WO 2012 / 174055, the contents of which are incorporated herein by reference in their entirety. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used to reduce or eliminate such complement activation and promote wound healing.Treatment with C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof may be carried out according to any of the methods for treating wounds disclosed in WO 2012 / 174055, the contents of which are incorporated herein by reference in their entirety.

[0129] brain trauma The wound and / or injury may include a head injury. Head trauma includes injury to the scalp, skull, or brain. Examples of head trauma include, but are not limited to, concussion, contusion, skull fracture, traumatic brain injury, and / or other injuries. Head trauma may be mild or severe. In some cases, head trauma may cause long-term physical and / or mental complications or death. Studies have shown that head trauma can induce inappropriate activation of the intracranial complement cascade, which can cause a local inflammatory response that contributes to secondary brain damage through the development of cerebral edema and / or neuronal death (Stahel et al., Brain Research Reviews, 1998, 27:243-56, the contents of which are incorporated herein by reference in their entirety). In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein may be used to treat head trauma and / or prevent or delay the onset of diseases, disorders, and / or conditions associated with head trauma. In some embodiments, the complement inhibitor compounds and compositions may be used to treat, prevent, reduce, or delay the onset of secondary complications of head trauma. Methods of using complement inhibitor compounds and compositions to control complement cascade activation in head trauma may include any of those taught in Holers et al., U.S. Pat. No. 8,911,733, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat head trauma and / or prevent or delay the onset of diseases, disorders, and / or conditions associated with head trauma. In some embodiments, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used to treat, prevent, reduce, or delay the onset of secondary complications of head trauma.Methods for controlling complement cascade activation in head trauma using C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may include any of those taught in Holers et al., U.S. Pat. No. 8,911,733, the contents of which are incorporated herein by reference in their entirety.

[0130] crush injury The wound and / or injury may include a crush injury. A crush injury is an injury caused by force or pressure applied to the body, resulting in bleeding, bruising, fractures, nerve damage, wounds, and / or other injuries to the body. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat and / or promote healing of crush injuries. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat and / or promote healing of crush injuries. Treatment may be used to reduce complement activation after a crush injury, thereby promoting healing after a crush injury (e.g., by promoting nerve regeneration, promoting fracture healing, preventing or treating inflammation and / or other related complications). The complement inhibitor compounds and / or compositions thereof described herein may be used to promote healing according to any of the methods taught in U.S. Pat. No. 8,703,136; WO 2012 / 162215; WO 2012 / 174055; or U.S. Patent Application Publication No. 2006 / 0270590, the contents of each of which are incorporated herein by reference in their entireties. C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof may be used to promote healing according to any of the methods taught in U.S. Pat. No. 8,703,136; WO 2012 / 162215; WO 2012 / 174055; or U.S. Patent Application Publication No. 2006 / 0270590, the contents of each of which are incorporated herein by reference in their entireties.

[0131] Autoimmune Indications Therapeutic indications addressed by the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein may include autoimmune indications. As used herein, the term "autoimmune indication" refers to any therapeutic indication involving immune targeting of a subject's tissues and / or substances by the subject's own immune system. Autoimmune indications may include complement-related indications. Autoimmune indications may involve specific tissues or organs of the body. The immune system can be divided into innate and adaptive systems, which refer to nonspecific immediate defense mechanisms and more complex antigen-specific systems, respectively. The complement system is part of the innate immune system, which recognizes and eliminates pathogens. In addition, complement proteins may regulate adaptive immunity and link innate and adaptive responses. The complement inhibitor compounds and compositions of the present disclosure may be used to modulate complement in the treatment and / or prevention of autoimmune diseases. In some cases, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof can be used according to the methods set forth in Ballanti et al., Immunol Res. 2013, 56:477-491, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the autoimmune indication includes myasthenia gravis.

[0132] Therapeutic indications addressed by the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and / or compositions of the present disclosure can include autoimmune indications. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) can be used according to the methods set forth in Ballanti et al., Immunol Res. 2013, 56:477-491, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the autoimmune indication includes myasthenia gravis.

[0133] Antiphospholipid syndrome (APS) and catastrophic antiphospholipid syndrome (CAPS) Autoimmune indications may include antiphospholipid syndrome (APS). APS is an autoimmune condition caused by antiphospholipid antibodies, which cause blood to clot. APS can cause recurrent venous or arterial thrombosis in organs and complications in the placental circulation, leading to pregnancy-related complications such as miscarriage, stillbirth, preeclampsia, preterm birth, and / or other complications. Catastrophic antiphospholipid syndrome (CAPS) is an extreme and acute version of a similar condition that simultaneously causes venous blockage in several organs. Studies suggest that complement activation may contribute to APS-related complications, including pregnancy-related complications, thrombotic (clotting) complications, and vascular complications. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of APS and / or APS-related complications. In some embodiments, the complement inhibitor compounds and / or compositions thereof described herein can be used to prevent and / or treat APS by regulating complement activation. In some cases, the complement inhibitor compounds and / or compositions thereof described herein can be used to treat APS and / or APS-related complications according to the methods taught in Salmon et al., Ann Rheum Dis, 2002, 61(Suppl II):ii46-ii50, and Mackworth-Young, Clin Exp Immunol, 2004, 136, pp. 393-401, the contents of which are incorporated herein by reference in their entireties. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan, and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of APS and / or APS-related complications.In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan, and / or its active metabolites or variants) and compositions of the present disclosure may be used to prevent and / or treat APS through control of complement activation. In some cases, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan, and / or its active metabolites or variants) and compositions thereof may be used to prevent and / or treat APS, as described in Salmon et al., Annals of Rheumatic Diseases, the contents of which are incorporated herein by reference in their entirety. Rheum Dis, 2002, 61(Suppl II):ii46-ii50 and Mackworth-Young, Clin Exp Immunol, 2004, 136, pp. 393-401, may be used to treat APS and / or APS-related complications.

[0134] cold agglutinin disease Autoimmune indications may include cold agglutinin disease (CAD), also known as cold agglutinin-mediated hemolysis. CAD is an autoimmune disease caused by high concentrations of IgM antibodies interacting with red blood cells in the hypothermic range (Engelhardt et al., Blood, 2002, 100(5), pp. 1922-23). CAD may cause symptoms such as anemia, fatigue, dyspnea, hemoglobinuria, and / or acrocyanosis. CAD is associated with robust complement activation, and studies have shown that CAD can be treated with complement inhibitor therapy. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of CAD. Such use may treat CAD by inhibiting complement activity. In some cases, the complement inhibitor compounds and / or compositions thereof described herein may be used to treat CAD according to the methods taught in Roth et al., Blood, 2009, 113:3885-86, or WO 2012 / 139081, the contents of each of which are incorporated herein by reference in their entireties. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of CAD. Such uses may treat CAD by inhibiting complement activity. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used to treat CAD according to the methods taught in Roth et al., Blood, 2009, 113:3885-86, or WO 2012 / 139081, the contents of each of which are incorporated herein by reference in their entireties.

[0135] skin diseases Autoimmune indications can include skin diseases. The skin plays a role in the spectrum of immunological reactions and is associated with abnormal or overactivated complement protein function. Autoimmune mechanisms mediated by autoantibodies and the cytotoxic function of complement affect epithelial or vascular cells, causing tissue damage and skin inflammation (Palenius and Meri, Front Med (Lausanne), 2015, Vol. 2, p. 3). Skin diseases associated with autoimmune and complement disorders include, but are not limited to, hereditary and acquired angioedema, autoimmune urticaria (hives), systemic lupus erythematosus, vasculitic syndromes and urticarial vasculitis, bullous dermatoses (e.g., pemphigus, bullous pemphigoid, mucous membrane pemphigoid, epidermolysis bullosa acquisita, dermatitis herpetiformis, pemphigoid of pregnancy, and partial lipodustrophy). In some cases, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof described herein can be used to treat skin conditions such as psoriasis, psoriasis, and rheumatoid arthritis (rheumatoid arthritis), as described by Palenius and Meri, Frontiers in Medicine, the contents of which are incorporated herein by reference in their entirety. Autoimmune skin diseases may be treated according to the methods taught in Frontiers in Medicine (Lausanne), 2015, Vol. 2, p. 3. In some embodiments, the complement inhibitor compounds and / or compositions thereof described herein may be used to treat, prevent, or delay the onset of skin diseases. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used to treat autoimmune skin diseases according to the methods taught in Palenius and Meri, Frontiers in Medicine (Lausanne), 2015, Vol. 2, p. 3, the contents of which are incorporated herein by reference in their entirety.In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of skin disorders.

[0136] Pulmonary indications Therapeutic indications addressed by the compounds and / or compositions of the present disclosure may include pulmonary indications. As used herein, the term "pulmonary indication" refers to any therapeutic indication related to the lungs and / or associated airways. Pulmonary indications may include complement-related indications. Pulmonary indications may include, but are not limited to, asthma, pulmonary fibrosis, chronic obstructive pulmonary disease (COPD), and acute respiratory distress syndrome. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of pulmonary indications. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of pulmonary indications.

[0137] Chronic obstructive pulmonary disease (COPD) Pulmonary indications may include chronic obstructive pulmonary disease (COPD). COPD refers to a class of disorders associated with progressive pulmonary dysfunction, most commonly characterized by shortness of breath. Complement dysfunction has been implicated as a contributor to some pulmonary indications associated with COPD (Pandya, PH et al., 2013, Translational Review, Vol. 51(4), pp. 467-467, the contents of which are incorporated herein by reference in their entirety). In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of COPD. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of COPD.

[0138] Cardiovascular indications Therapeutic indications addressed by the compounds and / or compositions of the present disclosure may include cardiovascular indications. As used herein, the term "cardiovascular indication" refers to any therapeutic indication related to the heart and / or vasculature. Cardiovascular indications may include complement-related indications. Cardiovascular indications may include, but are not limited to, conditions resulting from atherosclerosis, myocardial infarction, stroke, vasculitis, trauma, and cardiovascular interventions (including, but not limited to, cardiac bypass surgery, arterial grafts, and angioplasty). In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein may be used to treat, prevent, or delay the onset of cardiovascular indications. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of cardiovascular indications.

[0139] Vascular indications are cardiovascular indications associated with blood vessels (e.g., arteries, veins, and capillaries). Such indications may affect blood circulation, blood pressure, blood flow, organ function, and / or other bodily functions. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of vascular indications. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of vascular indications.

[0140] coagulation In some embodiments, cardiovascular indications include therapeutic indications related to coagulation, the coagulation cascade, and / or components of the coagulation cascade. Historically, the complement activation pathway was considered separate from the coagulation cascade, but the interplay between these two systems has been more recently recognized. To maintain homeostasis, coagulation and complement are coordinately activated in an overlapping spatiotemporal manner in response to common pathophysiological stimuli. Diseases can manifest with unrestrained activation of innate immune and coagulation responses. Examples include, for example, atherosclerosis, stroke, coronary heart disease, diabetes, ischemia-reperfusion injury, trauma, paroxysmal nocturnal hemoglobinuria, age-related macular degeneration, and atypical hemolytic uremic syndrome.

[0141] Several molecular links between complement and coagulation are now recognized. For example, thrombin was found to promote complement activation by cleaving C5 (Huber-Lang et al., 2006, Nature Medicine). Med., Vol. 12(6), pp. 682-687; the contents of which are incorporated herein by reference in their entirety. Although thrombin has the ability to cleave C5 at R751 (to generate C5a and C5b), it more efficiently cleaves C5 at the highly conserved R947 site, resulting in C5T and C5b T Produces intermediate C5b T C5b interacts with other complement proteins and has significantly more lytic activity than C5b-9. T -9 membrane attack complex (Krisinger et al., 2014, Blood, 120(8), pp. 1717-1725).

[0142] Complement can be activated by additional components of the coagulation and / or inflammatory cascades. For example, other serine proteases with slightly different substrate specificities may act similarly. Huber-Lang et al. (2006) showed that thrombin not only cleaves C5 but also generates C3a in vitro when incubated with native C3 (Huber-Lang et al., 2006, Nature Med. 12(6):682-687). Similarly, other components of the coagulation pathway, such as FXa, FXIa, and plasmin, have been found to cleave both C5 and C3.

[0143] Specifically, it has been observed that plasmin, FXa, FIXa, and FXIa can cleave C5 to generate C5a and C5b in a mechanism similar to that observed with thrombin activation (Amara et al., 2010, J. Immunol. 185:5628-5636; Amara et al., 2008, Current Topics in Complement II, edited by J.D. Lambris, pp.71-79). The resulting anaphylatoxins were found to be biologically active, as demonstrated by dose-dependent chemotactic responses in neutrophils and HMC-1 cells, respectively. Plasmin-induced cleavage activity could be blocked in a dose-dependent manner by the serine protease inhibitors aprotinin and leupeptin. These findings suggest that various serine proteases belonging to the coagulation system can activate the complement cascade independently of the established pathway. Furthermore, functional C5a and C3a (as detected by immunoblot and ELISA) are generated, both of which are known to be highly involved in inflammatory responses.

[0144] In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat cardiovascular indications associated with coagulation, the coagulation cascade, and / or coagulation cascade components. Coagulation cascade components may include, but are not limited to, tissue factor, thrombin, FXa, FIXa, FXIa, plasmin, or other coagulation proteases. The compounds described herein and / or compositions thereof may be used to treat complement activation and / or coagulation (e.g., thrombosis) associated with such cardiovascular indications. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat cardiovascular indications associated with coagulation, the coagulation cascade, and / or coagulation cascade components. Coagulation cascade components may include, but are not limited to, tissue factor, thrombin, FXa, FIXa, FXIa, plasmin, or other coagulation proteases. The C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and / or compositions of the present disclosure may be used to treat complement activation and / or coagulation (e.g., thrombosis) associated with such cardiovascular indications.

[0145] Thrombotic microangiopathy (TMA) Vascular indications can include thrombotic microangiopathy (TMA) and related disorders. Microangiopathy affects the body's small blood vessels (capillaries), causing the capillary walls to thicken, weaken, and become prone to bleeding and slowed blood circulation. TMA tends to result in vascular thrombosis, endothelial cell damage, thrombocytopenia, and the development of hemolysis. Organs such as the brain, kidneys, muscles, gastrointestinal system, skin, and lungs can be affected. TMA can result from medical surgery and / or conditions including, but not limited to, hematopoietic stem cell transplant (HSCT), kidney damage, diabetes, and / or other conditions. TMA is described in Meri et al., European Journal of Internal Medicine, the contents of which are incorporated herein by reference in their entirety. As described in the Journal of Internal Medicine, 2013, Vol. 24, pp. 496-502, TMA may be caused by an underlying complement system dysfunction. Generally, TMA may result from increased levels of specific complement components that cause thrombosis. In some cases, this may be due to mutations in complement proteins or related enzymes. The resulting complement dysfunction may cause complement targeting of endothelial cells and platelets, leading to increased thrombosis. In some embodiments, TMA may be prevented and / or treated with a complement inhibitor compound (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or a composition thereof described herein. In some cases, methods for treating TMA with a complement inhibitor compound and / or a composition thereof described herein may be performed according to those described in U.S. Patent Application Publication No. 2012 / 0225056 or U.S. Patent Application Publication No. 2013 / 0246083, the contents of each of which are incorporated herein by reference in their entireties. In some embodiments, TMA can be prevented and / or treated with the disclosed C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions. In some cases, methods for treating TMA with the disclosed C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions can be carried out according to those described in U.S. Patent Application Publication No. 2012 / 0225056 or U.S. Patent Application Publication No. 2013 / 0246083, the contents of each of which are incorporated herein by reference in their entireties.

[0146] Disseminated intravascular coagulation (DIC) Vascular indications may include disseminated intravascular coagulation (DIC). DIC is a pathological condition in which the coagulation cascade in the blood is activated extensively, resulting in the formation of blood clots, particularly within capillaries. DIC can cause obstructive blood flow in tissues and ultimately damage organs. In addition, DIC can affect the normal process of blood clotting, resulting in severe bleeding. The complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or reduce the severity of DIC by modulating complement activity. In some cases, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used according to any of the methods for treating DIC taught in U.S. Pat. No. 8,652,477, the contents of which are incorporated herein by reference in their entirety. The C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or reduce the severity of DIC by modulating complement activity. In some cases, the C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used in accordance with any of the methods for treating DIC taught in U.S. Patent No. 8,652,477, the contents of which are incorporated herein by reference in their entirety.

[0147] vasculitis Vascular indications can include vasculitis. Generally, vasculitis is a disorder associated with inflammation of blood vessels, including veins and arteries, characterized by white blood cells attacking tissue and causing swelling of the blood vessels. Vasculitis can be associated with infection, such as Rocky Mountain spotted fever, or autoimmunity. An example of autoimmune-related vasculitis is antineutrophil cytoplasmic autoantibody (ANCA) vasculitis. ANCA vasculitis is caused by abnormal antibodies that attack the body's own cells and tissues. ANCA attacks the cytoplasm of certain white blood cells and neutrophils, causing them to attack the walls of blood vessels in certain organs and tissues of the body. ANCA vasculitis can affect the skin, lungs, eyes, and / or kidneys. Studies suggest that ANCA disease produces specific complement components that activate the alternative complement pathway, creating an inflammatory amplification loop that results in vascular damage (Jennette et al., 2013, Seminars in Nephrol. 33(6):557-64, the contents of which are incorporated herein by reference in their entirety). In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to prevent and / or treat vasculitis. In some cases, the complement inhibitor compounds described herein and / or compositions thereof may be used to prevent and / or treat ANCA vasculitis by inhibiting complement activation. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to prevent and / or treat vasculitis. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used to prevent and / or treat ANCA vasculitis by inhibiting complement activation.

[0148] Neurological indications Therapeutic indications addressed with the compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may include neurological indications. As used herein, the term "neurological indication" refers to any therapeutic indication related to the nervous system. Neurological indications may include complement-related indications. Neurological indications may include neurodegeneration. Neurodegeneration generally relates to the deterioration of neuronal structure or function, including neuronal death. In some embodiments, the complement inhibitor compounds described herein and / or compositions thereof may be used to treat, prevent, or delay the onset of neurological indications, including, but not limited to, neurodegenerative diseases and related disorders. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of neurological indications, including, but not limited to, neurodegenerative diseases and related disorders. Treatment can include inhibiting the effects of complement activity on neuronal cells using the compounds and compositions of the present disclosure. Neurodegenerative disorders include, but are not limited to, amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), Parkinson's disease, Alzheimer's disease, and Lewy body disease. In some embodiments, complement-related neurological indications include myasthenia gravis.

[0149] Amyotrophic lateral sclerosis (ALS) Neurological indications may include ALS, a fatal motor neuron disease characterized by degeneration of spinal cord neurons, the brainstem, and the motor cortex. ALS causes muscle weakness and ultimately respiratory failure. Complement dysfunction may contribute to ALS, and therefore ALS may be prevented, treated, and / or symptoms may be reduced by treatment with a complement inhibitor compound described herein (e.g., a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or a composition thereof that targets complement activity. In some embodiments, the complement inhibitor compound described herein and / or a composition thereof may be used to treat, prevent, or delay the onset of ALS and / or promote neuronal regeneration. In some cases, the complement inhibitor compounds and / or compositions thereof described herein can be used as complement inhibitors according to any of the methods taught in U.S. Patent Application Publication No. 2014 / 0234275 or U.S. Patent Application Publication No. 2010 / 0143344, the contents of each of which are incorporated herein by reference in their entireties. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure can be used to treat, prevent, or delay the onset of ALS and / or promote neuronal regeneration. In some cases, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions can be used as complement inhibitors according to any of the methods taught in U.S. Patent Application Publication No. 2014 / 0234275 or U.S. Patent Application Publication No. 2010 / 0143344, the contents of each of which are incorporated herein by reference in their entireties.

[0150] Alzheimer's disease Neurological indications may include Alzheimer's disease, a chronic neurodegenerative disorder with symptoms that may include disorientation, memory loss, mood swings, behavioral disturbances, and ultimately a decline in physical function. Alzheimer's disease is thought to be caused by extracellular brain deposition of amyloid associated with inflammation-related proteins, such as complement proteins (Sjoberg et al., 2009, Trends in Immunology, 30(2):83-90, the contents of which are incorporated herein by reference in their entirety). In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of Alzheimer's disease by controlling complement activity. In some cases, the complement inhibitor compounds and / or compositions thereof described herein can be used according to any of the methods for treating Alzheimer's disease taught in U.S. Patent Application Publication No. 2014 / 0234275, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure can be used to treat, prevent, or delay the onset of Alzheimer's disease by controlling complement activity. In some cases, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof can be used according to any of the methods for treating Alzheimer's disease taught in U.S. Patent Application Publication No. 2014 / 0234275, the contents of which are incorporated herein by reference in their entirety.

[0151] Multiple sclerosis and neuromyelitis optica Neurological indications may include multiple sclerosis (MS) or neuromyelitis optica (NMO). MS is an inflammatory condition that affects the central nervous system when the immune system launches an attack against the body's own tissues, particularly the myelin sheath that insulates the nerves. The condition may be caused by unknown environmental pathogens, such as viruses. MS is progressive and ultimately leads to the breakdown of communication between the brain and the rest of the body. Typical early symptoms include blurred vision, partial blindness, muscle weakness, impaired coordination and balance, movement disorders, pain, and speech disorders. NMO (also known as Devic's disease) is an inflammatory demyelinating disease that affects the optic nerve and spinal cord when the immune system attacks astrocytes. NMO is sometimes considered a variant of MS. Typical symptoms of NMO include muscle weakness or paralysis in the lower limbs, loss of sensation (e.g., blindness), and bladder and bowel dysfunction.

[0152] MS and NMO have been linked to complement component regulation, for example, through pathology and animal model studies (Ingram et al., Clin Exp Immunol., February 2009, Vol. 155(2): pp. 128-139). In the central nervous system, glial cells and neurons produce the majority of complement proteins, and their expression increases in response to inflammation. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitor, C5 inhibitor polypeptide, C5 inhibitor cyclic polypeptide, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof can be used to treat, prevent, or delay the onset of MS or NMO. Methods of treatment may include any of those taught in Ingram et al., Clin Exp Immunol., February 2009, Vol. 155(2), pp. 128-139, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of MS or NMO. Methods of treatment may include any of those taught in Ingram et al., Clin Exp Immunol., February 2009, Vol. 155(2), pp. 128-139, the contents of which are incorporated herein by reference in their entirety.

[0153] myasthenia gravis Neurological indications may include myasthenia gravis. Myasthenia gravis (MG) is a rare, complement-mediated autoimmune disease characterized by the production of autoantibodies targeting proteins critical for the normal transmission of chemical or neurotransmitter signals from nerves to muscles, such as acetylcholine receptor (AChR) proteins. The presence of AChR autoantibodies in patient samples may be used as an indicator of disease. The term "MG" herein encompasses all forms of MG. While approximately 15% of patients have symptoms limited to the ocular muscles, the majority of patients experience generalized myasthenia gravis. The term "generalized myasthenia gravis" or "gMG" herein refers to MG affecting multiple muscle groups throughout the body. While the prognosis for MG is generally benign, 10% to 15% of patients experience refractory MG. The term "refractory MG" or "rMG" herein refers to MG in which disease control cannot be achieved with current treatments or when immunosuppressive therapy results in severe side effects. This severe form of MG affects approximately 9,000 individuals in the United States.

[0154] Patients with MG characteristically exhibit muscle weakness that becomes more severe with repeated use and resolves with rest. Muscle weakness may be localized to specific muscles, such as those involved in eye movement, but often progresses to more diffuse weakness. Furthermore, MG can become life-threatening if the weakness involves the diaphragm and other chest wall muscles involved in breathing. This is the most feared complication of MG, known as myasthenic crisis or MG crisis, and requires hospitalization, intubation, and mechanical ventilation. Approximately 15% to 20% of patients with MG experience a myasthenic crisis within 2 years of diagnosis.

[0155] The most common target of autoantibodies in MG is the acetylcholine receptor, or AChR, located at the neuromuscular junction, where motor neurons transmit signals to skeletal muscle fibers. Current treatments for gMG focus on either enhancing AChR signaling or nonspecifically suppressing the autoimmune response. The first-line therapy for symptomatic gMG is treatment with acetylcholinesterase inhibitors, such as pyridostigmine, which is the only approved treatment for MG. Pyridostigmine monotherapy is sometimes sufficient to control mild ocular symptoms but is usually insufficient to treat generalized weakness, and administration of this therapy can be limited by cholinergic side effects. Therefore, in patients who remain symptomatic despite pyridostigmine therapy, corticosteroids, with or without systemic immunosuppressants, are indicated (Sanders DB et al., 2016, Neurology 87(4):419-25). Immunosuppressants used in gMG include azathioprine, cyclosporine, mycophenolate mofetil, methotrexate, tacrolimus, cyclophosphamide, and rituximab. To date, efficacy data for these agents are sparse, and no steroid-based or immunosuppressive therapy has been approved for the treatment of gMG. Furthermore, all of these agents are associated with well-documented long-term toxicities. Surgical removal of the thymus may be recommended in patients with non-thymoma gMG and moderate to severe symptoms in an attempt to reduce AChR autoantibody production (Wolfe GI et al., 2016, N Engl J Med., 375(6):511-512). Intravenous (IV) immunoglobulin and plasma exchange are usually restricted to short-term use in patients with myasthenic crisis or life-threatening indications, such as respiratory failure or dysphagia (Sanders et al., 2016).

[0156] Substantial evidence supports a role for the terminal complement cascade in the pathogenesis of AChR autoantibody-positive gMG. Results from animal models of experimental autoimmune MG indicate that autoantibody immune complex formation at the neuromuscular junction triggers activation of the classical complement pathway, leading to local activation of C3 and deposition of the membrane attack complex (MAC) at the neuromuscular junction, resulting in signal transduction defects and eventual muscle weakness (Kusner LL et al., 2012, Annals of the New York Academy of Sciences, NY Acad. Sci., Vol. 1274 (No. 1), pp. 127-32).

[0157] Binding of anti-AChR autoantibodies to muscle endplates leads to activation of the classical complement cascade and deposition of MAC on postsynaptic muscle fibers, causing local damage to the muscle membrane and reduced responsiveness of the muscle to neuronal stimulation.

[0158] In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof may be used to treat, prevent, or delay the onset of MG (e.g., gMG and / or rMG). Inhibition of complement activity may be used to block complement-mediated damage resulting from MG (e.g., gMG and / or rMG). In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or active metabolites or variants thereof) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of MG (e.g., gMG and / or rMG). Inhibition of complement activity may be used to block complement-mediated damage resulting from MG (e.g., gMG and / or rMG).

[0159] Kidney-related indications Therapeutic indications addressed by the compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can include kidney-related indications. As used herein, the term "kidney-related indication" refers to any therapeutic indication involving the kidney. Kidney-related indications can include complement-related indications. The kidneys are organs responsible for removing metabolic waste products from the bloodstream. They regulate blood pressure, the urinary system, and homeostatic functions and are therefore essential for various bodily functions. Due to their unique structural features and exposure to blood, the kidneys can be more severely affected by inflammation (compared to other organs). The kidneys also produce their own complement proteins, which can be activated in response to infection, kidney disease, and kidney transplantation. In some embodiments, the complement inhibitor compounds described herein and / or compositions thereof can be used to treat, prevent, or delay the onset of kidney-related indications, in some cases by inhibiting complement activity. In some cases, the complement inhibitor compounds and / or compositions thereof described herein may be used to treat kidney-related indications according to the methods taught in Quigg, J Immunol, 2003, 171:3319-24, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of kidney-related indications in some cases by inhibiting complement activity. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions may be used to treat kidney-related indications according to the methods taught in Quigg, J Immunol, 2003, 171:3319-24, the contents of which are incorporated herein by reference in their entirety.

[0160] Atypical hemolytic uremic syndrome (aHUS) Kidney-related indications can include atypical hemolytic uremic syndrome (aHUS). aHUS belongs to the spectrum of thrombotic microangiopathy. aHUS is a condition that causes abnormal blood clot formation in the small blood vessels of the kidney. The condition is generally characterized by hemolytic anemia, thrombocytopenia, and renal failure, leading to end-stage renal disease (ESRD) in approximately half of all cases. aHUS is associated with defects in the alternative pathway of the complement system and can be caused by genetic mutations in one of the genes that cause increased activation of the alternative pathway (Verhave et al., Nephrol Dial Transplant 2014, Vol. 29, Suppl 4:iv131-41 and WO 2016 / 138520). aHUS can be treated with inhibitors that regulate the alternative pathway of complement activation, including C5 activation. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can be used to treat, prevent, or delay the onset of aHUS. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure can be used to treat, prevent, or delay the onset of aHUS. Methods and compositions for preventing and / or treating aHUS through complement inhibition can include any of those taught in Verhave et al., Nephrol Dial Transplant 2014, Vol. 29, Suppl 4:iv131-41, or WO 2016 / 138520, the contents of each of which are incorporated herein by reference in their entireties.

[0161] Lupus nephritis Kidney-related indications may include lupus nephritis. Lupus nephritis is nephritis caused by an autoimmune disease called systemic lupus erythematosus (SLE). Symptoms of lupus nephritis include high blood pressure; foamy urine; swelling of the legs, feet, hands, or face; joint pain; muscle pain; fever; and rash. In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein may be used to treat, prevent, or delay the onset of lupus nephritis, in some cases, by inhibiting complement activity. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions disclosed herein may be used to treat, prevent, or delay the onset of lupus nephritis, in some cases, by inhibiting complement activity. Related methods may include any of those taught in U.S. Patent Application Publication No. 2013 / 0345257 or U.S. Patent No. 8,377,437, the contents of each of which are incorporated herein by reference in their entirety.

[0162] Membranous glomerulonephritis (MGN) Kidney-related indications can include membranous glomerulonephritis (MGN). MGN is a kidney disorder that can cause inflammation and structural changes. MGN is caused by antibodies binding to soluble antigens in the kidney capillaries (glomeruli). MGN can affect kidney functions, such as fluid filtration, and can lead to kidney failure. In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein can be used to treat, prevent, or delay the onset of MGN, e.g., by inhibiting complement activity. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions disclosed herein can be used to treat, prevent, or delay the onset of MGN, e.g., by inhibiting complement activity. Related treatment methods may include any of those taught in U.S. Patent Application Publication No. 2010 / 0015139 or WO 2000 / 021559, the contents of each of which are incorporated herein by reference in their entirety.

[0163] hemodialysis complications Kidney-related indications may include hemodialysis complications. Hemodialysis is a medical procedure used to maintain kidney function in subjects with renal failure. Hemodialysis involves external removal of waste products, such as creatinine, urea, and free water, from the blood. A common complication of hemodialysis treatment is chronic inflammation caused by contact between the blood and the dialysis membrane. Another common complication is thrombosis, which refers to the formation of blood clots that block blood circulation. Studies suggest that these complications are related to complement activation. Hemodialysis may be combined with complement inhibitor therapy to control inflammatory responses and pathology and / or provide a means to prevent or treat thrombosis in subjects undergoing hemodialysis due to renal failure. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of hemodialysis complications, for example, by inhibiting complement activation. In some embodiments, the C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of hemodialysis complications, for example, by inhibiting complement activation. Methods related to the treatment of hemodialysis complications may include any of those taught in DeAngelis et al., Immunobiology, 2012, 217(11), pp. 1097-1105, or Kourtzelis et al., Blood, 2010, 116(4), pp. 631-639, the contents of each of which are incorporated herein by reference in their entirety.

[0164] IgA nephropathy Kidney-related indications may include IgA nephropathy. IgA nephropathy is the most common cause of glomerulonephritis, affecting 25 out of every 1 million people per year. The disease is characterized by mesangial deposition of IgA and complement components in the glomeruli. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of IgA nephropathy by inhibiting the activation of specific complement components. The compounds and / or compositions thereof described herein may be used in combination with Maillard's steroids, the contents of each of which are incorporated herein by reference in their entirety. The C5-inhibiting cyclic polypeptides and compositions disclosed herein may be used in accordance with the method for preventing and / or treating IgA nephropathy through complement inhibition taught in Maillard N et al., J of Am Soc Nephrology, 2015, Vol. 26 (No. 7), pp. 1503-1512. In some embodiments, the C5-inhibiting cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of IgA nephropathy by inhibiting the activation of specific complement components. The C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used in accordance with the method for preventing and / or treating IgA nephropathy by complement inhibition taught in Maillard N et al., J of Am Soc Nephr, 2015, 26(7), pp. 1503-1512, the contents of each of which are incorporated herein by reference in their entireties.

[0165] Dense deposit disease / membranoproliferative glomerulonephritis type II / C3 glomerulopathy Kidney-related indications may include dense deposit disease, membranoproliferative glomerulonephritis type II, and C3 glomerulopathy. Dense deposit disease (DDD) is a complement-related indication involving kidney damage. DDD may include proteinuria, hematuria, decreased urine volume, low levels of protein in the blood, and swelling in many areas of the body. DDD may be caused by mutations in the C3 and CFH genes; by both genetic risk factors and environmental triggers; or by the presence of autoantibodies that block the activity of proteins necessary for the body's immune response. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of DDD. In some embodiments, the disclosed C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions can be used to treat, prevent, or delay the onset of DDD. Such uses can include reducing and / or blocking alternative complement pathway activity. Such methods can prevent glomerular C3 deposition.

[0166] Focal segmental glomerulosclerosis Kidney-related indications may include focal segmental glomerulosclerosis. Focal segmental glomerulosclerosis (FSGS) is a common cause of glomerular disease in children and adults, most commonly manifesting as severe nephrotic syndrome. The diagnosis of FSGS is based on histopathological findings and the exclusion of other common diagnoses in nephrotic syndrome. Many patients have substantial deposition of IgM and C3 in the sclerotic areas upon biopsy. Additionally, biomarkers for complement activation (factor B fragment, C4a, soluble MAC) have been detected in the plasma and urine of patients with FSGS, with levels of Ba and Bb correlating with disease severity (J. Thurman et al., PLOSone, 2015). In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of FSGS. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of FSGS.

[0167] Diabetes-related indications Therapeutic indications addressed by the compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can include diabetes-related indications. As used herein, the term "diabetes-related indications" refers to any therapeutic indication arising from or related to elevated blood glucose. Diabetes-related indications can include complement-related indications. Diabetes-related indications can occur as a result of exposure of organs and / or tissues to prolonged hyperglycemia. Prolonged hyperglycemia can result in glycative inactivation of the membrane-associated complement regulatory protein CD59, leaving certain cells and tissues vulnerable to complement attack (P. Ghosh et al., 2015, Endocrine Reviews, Vol. 36(3), 2015). Complement-mediated complications from diabetes may include, but are not limited to, diabetic neuropathy, diabetic nephropathy, diabetic cardiovascular disease, and complications resulting from gestational diabetes, such as high or low birth weight and the complications resulting therefrom. In some embodiments, the complement inhibitor compounds and / or compositions thereof described herein may be used to treat, prevent, or delay the onset of diabetes-related indications. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of diabetes-related indications. Such uses may include addressing diabetes-related indications through complement activity inhibition.

[0168] Ophthalmic indications Therapeutic indications addressed by the compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may include ophthalmic indications. As used herein, the term "ophthalmic indication" refers to any therapeutic indication related to the eye. Ophthalmic indications may include complement-related indications. In a healthy eye, the complement system is activated at low levels and is continuously regulated by membrane-bound and soluble intraocular proteins that protect against pathogens. Thus, complement activation plays an important role in several eye-related complications, and control of complement activation may be used to treat such diseases. In some embodiments, the complement inhibitor compounds described herein and / or compositions thereof may be used to treat, prevent, or delay the onset of ophthalmic indications, for example, by inhibiting complement activity. In some embodiments, the C5-inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of ocular indications, for example, by inhibiting complement activity. Related treatment methods may include any of those taught in Jha et al., Mol Immunol., 2007, 44(16), pp. 3901-3908, or U.S. Pat. No. 8,753,625, the contents of each of which are incorporated herein by reference in their entirety.

[0169] Ophthalmic indications may include, but are not limited to, age-related macular degeneration, allergic and giant papillary conjunctivitis, Behçet's disease, choroidal inflammation, complications associated with intraocular surgery, corneal graft rejection, corneal ulcers, cytomegalovirus retinitis, dry eye syndrome, endophthalmitis, Fuchs' disease, glaucoma, immune complex vasculitis, inflammatory conjunctivitis, ischemic retinal disease, keratitis, macular edema, ocular parasitic infection / migration, retinitis pigmentosa, scleritis, Stargardt's disease, subretinal fibrosis, uveitis, vitreoretinal inflammation, and Vogt-Koyanagi-Harada disease.

[0170] Age-related macular degeneration (AMD) Ophthalmic indications may include age-related macular degeneration (AMD). AMD is a chronic eye disease that causes blurring of central vision, blind spots in the central field, and / or eventual loss of central vision. Central vision affects the ability to read, drive, and / or recognize faces. AMD is generally divided into two types: non-exudative (dry) and exudative (wet). Dry AMD refers to the deterioration of the macula, the central tissue of the retina. Wet AMD refers to damage to the blood vessels under the retina, causing leakage of blood and fluid. Several human and animal studies have identified complement proteins associated with AMD, and novel therapeutic strategies have involved regulating the complement activation pathway, as discussed in Jha et al., Mol Immunol., 2007, 44(16):3901-3908. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of AMD by inhibiting complement activation in the eye. Methods of the present disclosure that include the use of the complement inhibitor compounds described herein and / or their compositions to prevent and / or treat AMD may include any of those taught in U.S. Patent Application Publication No. 2011 / 0269807 or U.S. Patent Application Publication No. 2008 / 0269318, the contents of each of which are incorporated herein by reference in their entireties. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of AMD by inhibiting complement activation in the eye. Methods of the present disclosure involving the use of C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof for preventing and / or treating AMD may include any of those taught in U.S. Patent Application Publication No. 2011 / 0269807 or U.S. Patent Application Publication No. 2008 / 0269318, the contents of each of which are incorporated herein by reference in their entirety.

[0171] Corneal disorders Ophthalmic indications may include corneal diseases. The complement system plays an important role in protecting the cornea from pathogenic particles and / or inflammatory antigens. The cornea is the outermost, anterior part of the eye, protecting the iris, pupil, and anterior chamber and therefore exposed to external elements. Corneal diseases include, but are not limited to, keratoconus, keratitis, ocular herpes simplex, and / or other diseases. Corneal complications may cause pain, blurred vision, tearing, redness, light sensitivity, and / or corneal scarring. While the complement system is critical for corneal protection, complement activation can cause damage to corneal tissue after infection is cleared when certain complement compounds are severely expressed. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of corneal diseases by inhibiting complement activation in the eye. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure may be used to treat, prevent, or delay the onset of corneal diseases by inhibiting complement activation in the eye. Methods of the present disclosure for modulating complement activity in the treatment of corneal diseases may include any of those taught in Jha et al., Mol Immunol., 2007, 44(16):3901-3908, the contents of which are incorporated herein by reference in their entirety.

[0172] Autoimmune uveitis Ophthalmic indications may include autoimmune uveitis. The uvea is the pigmented area of the eye, including the choroid, iris, and ciliary body. Uveitis can cause redness, blurred vision, pain, adhesions, and ultimately blindness. Studies have shown that complement activation products are present in the eyes of patients with autoimmune uveitis, and that complement plays an important role in disease development. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of uveitis. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions disclosed herein may be used to treat, prevent, or delay the onset of uveitis. Such treatment may be carried out according to any of the methods identified in Jha et al., Mol Immunol. 2007, 44(16):3901-8, the contents of which are incorporated herein by reference in their entirety.

[0173] diabetic retinopathy Ophthalmic indications may include diabetic retinopathy, a disease caused by changes in retinal blood vessels in diabetic patients. Retinopathy can cause vascular swelling and fluid leakage and / or abnormal blood vessel growth. Diabetic retinopathy can affect vision and ultimately lead to blindness. Studies suggest that complement activation plays an important role in the development of diabetic retinopathy. In some embodiments, the complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof may be used to treat, prevent, or delay the onset of diabetic retinopathy. The complement inhibitor compounds and / or compositions thereof described herein may be used in accordance with the method for treating diabetic retinopathy described in Jha et al., Mol Immunol., 2007, 44(16):3901-3908, the contents of which are incorporated herein by reference in their entirety. In some embodiments, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions of the present disclosure can be used to treat, prevent, or delay the onset of diabetic retinopathy. The C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions can be used according to the method for treating diabetic retinopathy described in Jha et al., Mol Immunol., 2007, 44(16):3901-3908, the contents of which are incorporated herein by reference in their entirety.

[0174] Stargardt disease Ophthalmic indications may include Stargardt disease. Stargardt disease, also known as recessive Stargardt macular degeneration, is a genetic disorder of the eye that typically begins within the first 20 years of life. Complications from Stargardt disease may include vision loss (Radu et al., J. Biol. Chem. 2011, 286(21):18593-18601). The disease is caused by a mutation in the ABCA4 gene. Disease hallmarks include the accumulation of lipofuscin, which has been shown to activate the complement cascade (Radu et al., J. Biol. Chem. 2011, 286(21):18593-18601). Furthermore, a study (Tan et al., Proceedings of the National Academy of Sciences of the United States of America (PNAS), 2016, Vol. 113 (31), pp. 8789-8794) also showed that ABCA4 gene mutations affect organelle transport, leading to the accumulation of lipofuscin, and downregulation of CD59 on the surface of RPE cells, making them more susceptible to damage from complement activation. In some embodiments, the complement inhibitor compounds (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions described herein can be used to treat, prevent, or delay the onset of Stargardt disease, e.g., by inhibiting complement activation in the eye. In some embodiments, the C5 inhibitor cyclic polypeptides (e.g., zilucoplan and / or their active metabolites or variants) and compositions disclosed herein can be used to treat, prevent, or delay the onset of Stargardt disease, e.g., by inhibiting complement activation in the eye.

[0175] Pregnancy-related indications Therapeutic indications addressed with the compounds and / or compositions of the present disclosure may include pregnancy-related indications. As used herein, the term "pregnancy-related indication" refers to any therapeutic indication involving childbirth and / or pregnancy. Pregnancy-related indications may include complement-related indications. Pregnancy-related indications may include preeclampsia and / or HELLP syndrome (an abbreviation for a syndrome characterized by 1) hemolysis, 2) elevated liver enzymes, and 3) low platelet counts. Preeclampsia is a disorder of pregnancy with symptoms including elevated blood pressure, swelling, shortness of breath, impaired kidney function, impaired liver function, and / or low platelet counts. Preeclampsia is typically diagnosed by elevated urinary protein levels and hypertension. HELLP syndrome is a combination of hemolysis, elevated liver enzymes, and low platelet counts. Hemolysis is a condition involving the rupture of red blood cells, which causes the release of hemoglobin from the red blood cells. Elevated liver enzymes may indicate a pregnancy-induced liver condition. Low platelet levels cause hypocoagulability, leading to the risk of excessive bleeding. HELLP is associated with preeclampsia and liver damage. HELLP syndrome typically occurs during the later stages of pregnancy or after birth. It is typically diagnosed by a blood test, which indicates the presence of three conditions it includes. HELLP is typically treated by inducing labor.

[0176] Studies suggest that complement activation occurs during HELLP syndrome and preeclampsia, and that certain complement components are present at increased levels during HELLP and preeclampsia. The complement inhibitor compounds described herein (e.g., C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can be used as therapeutic agents to prevent and / or treat these and other pregnancy-related indications. The complement inhibitor compounds and / or compositions thereof described herein can be used according to the methods for preventing and / or treating HELLP and preeclampsia taught in Heager et al., Obstetrics & Gynecology, 1992, Vol. 79(1), pp. 19-26, or WO 2014 / 078622, the contents of each of which are incorporated herein by reference in their entireties. The C5-inhibiting cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) of the present disclosure can be used as therapeutic agents to prevent and / or treat these and other pregnancy-related indications. The C5-inhibiting cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) and compositions thereof can be used in accordance with the methods for preventing and / or treating HELLP and pre-eclampsia taught in Heager et al., Obstetrics & Gynecology, 1992, Vol. 79(1), pp. 19-26, or WO 2014 / 078622, the contents of each of which are incorporated herein by reference in their entireties.

[0177] Dosage and Administration In some embodiments, the present disclosure provides methods for administering an active ingredient described herein (e.g., a therapeutic agent, a C5 inhibitor, a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or a composition thereof. The active ingredient may be administered using any of the sustained-release formulations described herein. The sustained-release formulation may be administered by subcutaneous injection. The sustained-release formulation may be administered weekly or biweekly. The active ingredient may be released from the sustained-release formulation after administration. The concentration of the active ingredient in the target tissue or fluid surrounding the administration site of the sustained-release formulation may exhibit a burst of less than 5%. The sustained-release formulation may be administered at a dosage sufficient to administer about 2 mg / kg to about 20 mg / kg of the active ingredient. When the active ingredient is zilucoplan, the sustained-release formulation may be administered at a dosage sufficient to administer about 100 mg to about 200 mg of zilucoplan.

[0178] In some embodiments, the present disclosure provides methods for administering a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant). The C5 inhibitory cyclic polypeptide can include zilucoplan and / or its metabolites and / or variants. The C5 inhibitory cyclic polypeptide can be administered using any of the sustained-release formulations described herein. The sustained-release formulation can be administered by subcutaneous injection. The sustained-release formulation can be administered weekly or biweekly. The C5 inhibitory cyclic polypeptide can be released from the sustained-release formulation after administration. The concentration of the C5 inhibitory cyclic polypeptide in the target tissue or fluid surrounding the site of administration of the sustained-release formulation can exhibit a burst of less than 5%. The sustained-release formulation can be administered at a dosage sufficient to administer about 2 mg / kg to about 20 mg / kg of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant). The sustained-release formulation can be administered at a dosage sufficient to administer about 100 mg to about 200 mg of zilucoplan.

[0179] In some embodiments, the present disclosure provides methods of reducing hemolysis in a subject by administering a C5 inhibitor described herein (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or a composition thereof. The C5 inhibitor may be administered as part of a sustained-release formulation described herein.

[0180] In some embodiments, the present disclosure provides methods for reducing hemolysis in a subject by administering a C5 inhibitory cyclic polypeptide described herein (e.g., zilucoplan and / or its active metabolite or variant). The C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) can be administered as part of a sustained release formulation described herein.

[0181] The C5 inhibitors described herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof can be provided in therapeutically effective amounts. In some cases, a therapeutically effective amount of a C5 inhibitor can be achieved by administering one or more C5 inhibitors in a dosage of about 0.1 mg to about 1 mg, about 0.5 mg to about 5 mg, about 1 mg to about 20 mg, about 5 mg to about 50 mg, about 10 mg to about 100 mg, about 20 mg to about 200 mg, or at least 200 mg.

[0182] C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) can be provided in therapeutically effective amounts. In some cases, a therapeutically effective amount of C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) can be achieved by administering a dosage of about 0.1 mg to about 1 mg, about 0.5 mg to about 5 mg, about 1 mg to about 20 mg, about 5 mg to about 50 mg, about 10 mg to about 100 mg, about 20 mg to about 200 mg, or at least 200 mg of one or more C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants).

[0183] In some embodiments, a subject may be administered a therapeutic amount of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) based on the subject's body weight. In some cases, the C5 inhibitor may be administered at a dose of about 0.001 mg / kg to about 1.0 mg / kg, about 0.01 mg / kg to about 2.0 mg / kg, about 0.05 mg / kg to about 5.0 mg / kg, about 0.03 mg / kg to about 3.0 mg / kg, about 0.01 mg / kg to about 10 mg / kg, about 0.1 mg / kg to about 2.0 mg / kg, about 0.2 mg / kg to about 3.0 mg / kg, about 0.4 mg / kg to about 4.0 mg / kg, about 1.0 mg / kg to about 5.0 mg / kg, about 2.0 mg / kg, or about 3.0 mg / kg. The drug may be administered at a dose of about 0.01 mg / kg to about 4.0 mg / kg, about 1.5 mg / kg to about 7.5 mg / kg, about 5.0 mg / kg to about 15 mg / kg, about 7.5 mg / kg to about 12.5 mg / kg, about 10 mg / kg to about 20 mg / kg, about 15 mg / kg to about 30 mg / kg, about 20 mg / kg to about 40 mg / kg, about 30 mg / kg to about 60 mg / kg, about 40 mg / kg to about 80 mg / kg, about 50 mg / kg to about 100 mg / kg, or at least 100 mg / kg. Such ranges may include those suitable for administration to human subjects. Dosage levels may be highly dependent on the nature of the condition, drug efficacy, patient condition, the judgment of the practitioner, and the frequency and mode of administration. In some embodiments, zilucoplan and / or its active metabolite or variant may be administered at a dose of about 0.01 mg / kg to about 10 mg / kg. In some cases, zilucoplan and / or its active metabolite or variant may be administered at a dosage of about 0.1 mg / kg to about 3 mg / kg.

[0184] In some embodiments, a subject may be administered a therapeutic amount of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) based on the subject's body weight. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) may be administered at a dose of about 0.001 mg / kg to about 1.0 mg / kg, about 0.01 mg / kg to about 2.0 mg / kg, about 0.05 mg / kg to about 5.0 mg / kg, about 0.03 mg / kg to about 3.0 mg / kg, about 0.01 mg / kg to about 10 mg / kg, about 0.1 mg / kg to about 2.0 mg / kg, about 0.2 mg / kg to about 3.0 mg / kg, about 0.4 mg / kg to about 4.0 mg / kg, about 1.0 mg / kg, or about 1.0 mg / kg. The compound may be administered at a dose of about 100 mg / kg to about 5.0 mg / kg, about 2.0 mg / kg to about 4.0 mg / kg, about 1.5 mg / kg to about 7.5 mg / kg, about 5.0 mg / kg to about 15 mg / kg, about 7.5 mg / kg to about 12.5 mg / kg, about 10 mg / kg to about 20 mg / kg, about 15 mg / kg to about 30 mg / kg, about 20 mg / kg to about 40 mg / kg, about 30 mg / kg to about 60 mg / kg, about 40 mg / kg to about 80 mg / kg, about 50 mg / kg to about 100 mg / kg, or at least 100 mg / kg. Such ranges may include those suitable for administration to human subjects. Dosage levels may be highly dependent on the nature of the condition; drug efficacy; the patient's condition; the practitioner's judgment; and the frequency and mode of administration. In some embodiments, zilucoplan and / or its active metabolite or variant may be administered at a dosage of about 0.01 mg / kg to about 10 mg / kg, or in some cases, zilucoplan and / or its active metabolite or variant may be administered at a dosage of about 0.1 mg / kg to about 3 mg / kg.

[0185] In some cases, the C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan and / or an active metabolite or variant thereof) is provided at a concentration adjusted to achieve a desired level of the C5 inhibitor in a sample, biological system, or subject (e.g., plasma level in the subject). In some cases, the desired concentration of the C5 inhibitor in a sample, biological system, or subject can include a concentration of about 0.001 μM to about 0.01 μM, about 0.005 μM to about 0.05 μM, about 0.02 μM to about 0.2 μM, about 0.03 μM to about 0.3 μM, about 0.05 μM to about 0.5 μM, about 0.01 μM to about 2.0 μM, about 0.1 μM to about 50 μM, about 0.1 μM to about 10 μM, about 0.1 μM to about 5 μM, about 0.2 μM to about 20 μM, about 5 μM to about 100 μM, or about 15 μM to about 200 μM. In some cases, the desired concentration of the C5 inhibitor in the subject's plasma can be about 0.1 μg / mL to about 1000 μg / mL. Desirable concentrations of C5 inhibitor in the subject's plasma include about 0.01 μg / mL to about 2 μg / mL, about 0.02 μg / mL to about 4 μg / mL, about 0.05 μg / mL to about 5 μg / mL, about 0.1 μg / mL to about 1.0 μg / mL, about 0.2 μg / mL to about 2.0 μg / mL, about 0.5 μg / mL to about 5 μg / mL, about 1 μg / mL to about 5 μg / mL, and about 2 μg / mL. The concentration may be from about 10 μg / mL to about 10 μg / mL, from about 3 μg / mL to about 9 μg / mL, from about 5 μg / mL to about 20 μg / mL, from about 10 μg / mL to about 40 μg / mL, from about 30 μg / mL to about 60 μg / mL, from about 40 μg / mL to about 80 μg / mL, from about 50 μg / mL to about 100 μg / mL, from about 75 μg / mL to about 150 μg / mL, or at least 150 μg / mL. In other embodiments, the C5 inhibitors described herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof provide a maximum C5 inhibitor serum concentration (C5) of at least 0.1 μg / mL, at least 0.5 μg / mL, at least 1 μg / mL, at least 5 μg / mL, at least 10 μg / mL, at least 50 μg / mL, at least 100 μg / mL, or at least 1000 μg / mL. max ) is administered at a dose sufficient to achieve

[0186] In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is provided at a concentration adjusted to achieve a desired level of the C5 inhibitor in a sample, biological system, or subject (e.g., plasma level in the subject). In some cases, the desired concentration of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) in a sample, biological system, or subject may include a concentration of about 0.001 μM to about 0.01 μM, about 0.005 μM to about 0.05 μM, about 0.02 μM to about 0.2 μM, about 0.03 μM to about 0.3 μM, about 0.05 μM to about 0.5 μM, about 0.01 μM to about 2.0 μM, about 0.1 μM to about 50 μM, about 0.1 μM to about 10 μM, about 0.1 μM to about 5 μM, about 0.2 μM to about 20 μM, about 5 μM to about 100 μM, or about 15 μM to about 200 μM. In some cases, the desired concentration of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) in a subject's plasma can be about 0.1 μg / mL to about 1000 μg / mL. The desired concentration of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) in a subject's plasma can be about 0.01 μg / mL to about 2 μg / mL, about 0.02 μg / mL to about 4 μg / mL, about 0.05 μg / mL to about 5 μg / mL, about 0.1 μg / mL to about 1.0 μg / mL, about 0.2 μg / mL to about 2.0 μg / mL, about 0.5 μg / mL to about 5 μg / mL, about 1 μg / mL to about 2 ... The concentration may be from about 100 μg / mL to about 5 μg / mL, from about 2 μg / mL to about 10 μg / mL, from about 3 μg / mL to about 9 μg / mL, from about 5 μg / mL to about 20 μg / mL, from about 10 μg / mL to about 40 μg / mL, from about 30 μg / mL to about 60 μg / mL, from about 40 μg / mL to about 80 μg / mL, from about 50 μg / mL to about 100 μg / mL, from about 75 μg / mL to about 150 μg / mL, or at least 150 μg / mL. In other embodiments, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) has a maximum serum concentration (C) of at least 0.1 μg / mL, at least 0.5 μg / mL, at least 1 μg / mL, at least 5 μg / mL, at least 10 μg / mL, at least 50 μg / mL, at least 100 μg / mL, or at least 1000 μg / mL.max ) is administered at a dose sufficient to achieve

[0187] In some embodiments, a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) is administered daily at a dose sufficient to deliver about 0.1 mg / day to about 60 mg / day per kg of the subject's body weight. In some embodiments, a C5 inhibitor cyclic polypeptide (e.g., zilucoplan and / or an active metabolite or variant thereof) is administered daily at a dose sufficient to deliver about 0.1 mg / day to about 60 mg / day per kg of the subject's body weight. In some cases, the C5 inhibitor achieved with each dose is max In such cases, the area under the curve (AUC) during administration can be from about 200 μg·hr / mL to about 10,000 μg·hr / mL.

[0188] According to some methods of the present disclosure, a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) is provided at a concentration required to achieve a desired effect. In some cases, the compounds and compositions of the present disclosure are provided in an amount required to reduce a given reaction or process by half. The concentration required to achieve such a reduction is referred to herein as the half maximal inhibitory concentration, or "IC 50 Alternatively, the compounds and compositions of the present disclosure may be provided in an amount required to increase a given reaction, activity, or process by half. The concentration required for such an increase is referred to herein as the half maximal effective concentration, or "EC 50 "It is called "

[0189] The C5 inhibitor (e.g., C5 inhibitor polypeptide, C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolite or variant) may be present in an amount that, in total, amounts to 0.1 to 95% by weight of the total weight of the composition. In some cases, the C5 inhibitor is administered intravenously (IV). In some cases, the C5 inhibitor is administered subcutaneously (SC).

[0190] The C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) may be present in an amount that totals 0.1 to 95% by weight of the total weight of the composition. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is provided by IV administration. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is provided by SC administration.

[0191] SC administration of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) may, in some cases, offer advantages over IV administration. SC administration allows patients to provide self-treatment. Such treatment can be advantageous in that patients can provide treatment themselves at home, avoiding the need to travel to a provider or medical facility. Furthermore, SC treatment allows patients to avoid long-term complications associated with IV administration, such as infection, loss of venous access, local thrombosis, and hematoma. In some embodiments, SC treatment may increase patient compliance, patient satisfaction, quality of life, and reduce treatment costs and / or drug requirements.

[0192] In some cases, daily SC administration provides a steady-state concentration of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) that is reached within 1 to 3 doses, 2 to 3 doses, 3 to 5 doses, or 5 to 10 doses. In some cases, a daily SC dose of about 0.1 mg / kg to about 0.3 mg / kg can achieve sustained C5 inhibitor levels of 2.5 μg / mL or greater and / or greater than 90% inhibition of complement activity.

[0193] In some cases, daily SC administration provides a steady-state concentration of C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) that is reached within 1 to 3 doses, 2 to 3 doses, 3 to 5 doses, or 5 to 10 doses. In some cases, daily SC doses of about 0.1 mg / kg to about 0.3 mg / kg can achieve sustained C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) levels of 2.5 μg / mL or greater and / or greater than 90% inhibition of complement activity.

[0194] C5 inhibitors (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) can exhibit slow absorption kinetics (observed times to peak concentration exceeding 4-8 hours) and high bioavailability (about 75% to about 100%) following SC administration.

[0195] C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) can exhibit slow absorption kinetics (observed times to peak concentration exceeding 4-8 hours) and high bioavailability (about 75% to about 100%) after SC administration.

[0196] In some embodiments, the dose and / or administration is modified to reduce the half-life (t1 / 2 ) is adjusted. In some cases, t 1 / 2 is at least 1 hour, at least 2 hours, at least 4 hours, at least 6 hours, at least 8 hours, at least 10 hours, at least 12 hours, at least 16 hours, at least 20 hours, at least 24 hours, at least 36 hours, at least 48 hours, at least 60 hours, at least 72 hours, at least 96 hours, at least 5 days, at least 6 days, at least 7 days, at least 8 days, at least 9 days, at least 10 days, at least 11 days, at least 12 days, at least 2 weeks, at least 3 weeks, at least 4 weeks, at least 5 weeks, at least 6 weeks, at least 7 weeks, at least 8 weeks, at least 9 weeks, at least 10 weeks, at least 11 weeks, at least 12 weeks, or at least 16 weeks.

[0197] In some embodiments, the dose and / or administration is modified to reduce the half-life (t 1 / 2 ) is adjusted. In some cases, t 1 / 2 is at least 1 hour, at least 2 hours, at least 4 hours, at least 6 hours, at least 8 hours, at least 10 hours, at least 12 hours, at least 16 hours, at least 20 hours, at least 24 hours, at least 36 hours, at least 48 hours, at least 60 hours, at least 72 hours, at least 96 hours, at least 5 days, at least 6 days, at least 7 days, at least 8 days, at least 9 days, at least 10 days, at least 11 days, at least 12 days, at least 2 weeks, at least 3 weeks, at least 4 weeks, at least 5 weeks, at least 6 weeks, at least 7 weeks, at least 8 weeks, at least 9 weeks, at least 10 weeks, at least 11 weeks, at least 12 weeks, or at least 16 weeks.

[0198] In some embodiments, the C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) induces a long terminal phase t 1 / 2 A long terminal phase may be observed. 1 / 2 This may be due to extensive target binding and / or additional plasma protein binding. In some cases, C5 inhibitors have been shown to increase t in both plasma and whole blood for more than 24 hours. 1 / 2 Values are shown. In some cases, C5 inhibitors do not lose functional activity after 16 hours of incubation in human whole blood at 37°C.

[0199] In some embodiments, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) exhibits a long terminal phase t 1 / 2 A long terminal phase may be observed. 1 / 2 This may be due to extensive target binding and / or additional plasma protein binding. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) exhibit a t of greater than 24 hours in both plasma and whole blood. 1 / 2 In some cases, the C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) do not lose functional activity after 16 hours of incubation in human whole blood at 37°C.

[0200] In some embodiments, the dose and / or administration is altered to modulate the steady-state volume of distribution of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof). In some cases, the steady-state volume of distribution of the C5 inhibitor is about 0.1 mL / kg to about 1 mL / kg, about 0.5 mL / kg to about 5 mL / kg, about 1 mL / kg to about 10 mL / kg, about 5 mL / kg to about 20 mL / kg, about 15 mL / kg to about 30 mL / kg, about 10 mL / kg to about 200 mL / kg, about 20 mL / kg to about 60 mL / kg, about 30 mL / kg to about 70 mL / kg, about 50 mL / kg to about 200 mL / kg, about 100 mL / kg to about 500 mL / kg, or at least 500 mL / kg. In some cases, the dose and / or administration of the C5 inhibitor is adjusted to ensure that the steady-state volume of distribution is at least 50% of the total blood volume, hi some embodiments, the C5 inhibitor distribution may be limited to the plasma compartment.

[0201] In some embodiments, the dose and / or administration is altered to modulate the steady-state volume of distribution of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant). In some cases, the steady-state volume of distribution of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is about 0.1 mL / kg to about 1 mL / kg, about 0.5 mL / kg to about 5 mL / kg, about 1 mL / kg to about 10 mL / kg, about 5 mL / kg to about 20 mL / kg, about 15 mL / kg to about 30 mL / kg, about 10 mL / kg to about 200 mL / kg, about 20 mL / kg to about 60 mL / kg, about 30 mL / kg to about 70 mL / kg, about 50 mL / kg to about 200 mL / kg, about 100 mL / kg to about 500 mL / kg, or at least 500 mL / kg. In some cases, the dose and / or administration of the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is adjusted to ensure a steady-state volume of distribution of at least 50% of the total blood volume. In some embodiments, C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) distribution may be limited to the plasma compartment.

[0202] In some embodiments, the C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) is administered at a dose of about 0.001 mL / hr / kg to about 0.01 mL / hr / kg, about 0.005 mL / hr / kg to about 0.05 mL / hr / kg, about 0.01 mL / hr / kg to about 0.1 mL / hr / kg, or about 0.05 mL / hr / kg to about The total clearance rate is 0.5 mL / hr / kg, about 0.1 mL / hr / kg to about 1 mL / hr / kg, about 0.5 mL / hr / kg to about 5 mL / hr / kg, about 0.04 mL / hr / kg to about 4 mL / hr / kg, about 1 mL / hr / kg to about 10 mL / hr / kg, about 5 mL / hr / kg to about 20 mL / hr / kg, about 15 mL / hr / kg to about 30 mL / hr / kg, or at least 30 mL / hr / kg.

[0203] In some embodiments, a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or an active metabolite or variant thereof) exhibits a total clearance rate of about 0.001 mL / hr / kg to about 0.01 mL / hr / kg, about 0.005 mL / hr / kg to about 0.05 mL / hr / kg, about 0.01 mL / hr / kg to about 0.1 mL / hr / kg, about 0.05 mL / hr / kg to about 0.5 mL / hr / kg, about 0.1 mL / hr / kg to about 1 mL / hr / kg, about 0.5 mL / hr / kg to about 5 mL / hr / kg, about 0.04 mL / hr / kg to about 4 mL / hr / kg, about 1 mL / hr / kg to about 10 mL / hr / kg, about 5 mL / hr / kg to about 20 mL / hr / kg, about 15 mL / hr / kg to about 30 mL / hr / kg, or at least 30 mL / hr / kg.

[0204] The time period (T) during which the maximum concentration of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) is maintained in a subject (e.g., in the subject's serum). max The T value can be adjusted by modifying the dose and / or administration (e.g., subcutaneous administration). In some cases, the C5 inhibitor has a T of about 1 minute to about 10 minutes, about 5 minutes to about 20 minutes, about 15 minutes to about 45 minutes, about 30 minutes to about 60 minutes, about 45 minutes to about 90 minutes, about 1 hour to about 48 hours, about 2 hours to about 10 hours, about 5 hours to about 20 hours, about 10 hours to about 60 hours, about 1 day to about 4 days, about 2 days to about 10 days, or at least 10 days. max It has a value.

[0205] The time period (T) during which the maximum concentration of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) in a subject (e.g., in the subject's serum) is maintained. maxThe T value can be adjusted by modifying the dose and / or administration (e.g., subcutaneous administration). In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) has a T of about 1 minute to about 10 minutes, about 5 minutes to about 20 minutes, about 15 minutes to about 45 minutes, about 30 minutes to about 60 minutes, about 45 minutes to about 90 minutes, about 1 hour to about 48 hours, about 2 hours to about 10 hours, about 5 hours to about 20 hours, about 10 hours to about 60 hours, about 1 day to about 4 days, about 2 days to about 10 days, or at least 10 days. max It has a value.

[0206] In some embodiments, the C5 inhibitors described herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can be administered without off-target effects. In some cases, the C5 inhibitors do not inhibit hERG (human ether-a-go-go related gene) even at concentrations of 300 μM or less. SC injections of C5 inhibitors with dose escalations up to 10 mg / kg can be well tolerated and do not result in any adverse cardiovascular (e.g., increased risk of prolonged ventricular repolarization) and / or respiratory effects.

[0207] In some embodiments, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) can be administered without off-target effects. In some cases, C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) do not inhibit hERG even at concentrations of 300 μM or less. SC injections of C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) with dose escalations up to 10 mg / kg can be well tolerated and do not result in any adverse cardiovascular (e.g., increased risk of prolonged ventricular repolarization) and / or respiratory effects.

[0208] The dosage of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) can be determined using the no-observed-adverse-effect level (NOAEL) observed in another species. Such species can include, but are not limited to, monkeys, rats, rabbits, and mice. In some cases, the human equivalent dose (HED) can be determined by allometric scaling from the NOAEL observed in other species. In some cases, the HED results in therapeutic margins of about 2-fold to about 5-fold, about 4-fold to about 12-fold, about 5-fold to about 15-fold, about 10-fold to about 30-fold, or at least 30-fold. In some cases, the therapeutic margin is determined by comparing the exposure in primates and the estimated human C5 in humans. max The level is determined by using

[0209] In some embodiments, the C5 inhibitors of the present disclosure (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) allow for rapid drug holiday in cases of infection where prolonged inhibition of the complement system would be detrimental.

[0210] Administration of the C5 inhibitors described herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or their active metabolites or variants) and / or compositions thereof can be adjusted to reduce potential clinical risks to a subject. Neisseria meningitidis infection is a known risk associated with C5 inhibitors, including eculizumab. In some cases, the risk of Neisseria meningitidis infection can be minimized by instituting one or more preventative steps. Such steps may include excluding subjects who may already be colonized with these bacteria. In some cases, preventative steps may include co-administration of one or more antibiotics. In some cases, ciprofloxacin may be co-administered. In some cases, ciprofloxacin may be co-administered orally at a dose of about 100 mg to about 1000 mg (e.g., 500 mg).

[0211] In some embodiments, the C5 inhibitors described herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof are administered hourly, every 2 hours, every 4 hours, every 6 hours, every 12 hours, every 18 hours, every 24 hours, every 36 hours, every 72 hours, every 84 hours, every 96 hours, every 5 days, every 7 days, every 10 days, every 14 days, weekly, every 2 weeks, every 3 weeks, every 4 weeks, monthly, every 2 months, every 3 months, every 4 months, every 5 months, every 6 months, yearly, or at least annually. In some cases, the C5 inhibitor is administered once daily or as two, three, or more sub-doses appropriately spaced throughout the day.

[0212] In some embodiments, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered hourly, every 2 hours, every 4 hours, every 6 hours, every 12 hours, every 18 hours, every 24 hours, every 36 hours, every 72 hours, every 84 hours, every 96 hours, every 5 days, every 7 days, every 10 days, every 14 days, weekly, every 2 weeks, every 3 weeks, every 4 weeks, monthly, every 2 months, every 3 months, every 4 months, every 5 months, every 6 months, yearly, or at least annually. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered once daily or as two, three, or more sub-doses appropriately spaced throughout the day.

[0213] In some embodiments, a C5 inhibitor described herein (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or composition thereof is administered in multiple daily doses. In some cases, the C5 inhibitor is administered daily for 7 consecutive days. In some cases, the C5 inhibitor described herein and / or composition thereof is administered daily for 7 to 100 consecutive days. In some cases, the C5 inhibitor described herein and / or composition thereof is administered daily for at least 100 consecutive days. In some cases, the C5 inhibitor described herein and / or composition thereof is administered daily indefinitely.

[0214] In some embodiments, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered in multiple daily doses. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered daily for 7 consecutive days. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered daily for 7 to 100 consecutive days. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered daily for at least 100 consecutive days. In some cases, the C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) is administered daily indefinitely.

[0215] Intravenously delivered C5 inhibitors described herein (e.g., C5 inhibitor polypeptides, C5 inhibitor cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof can be delivered by infusion over a period of time, such as over a period of 5, 10, 15, 20, or 25 minutes. Administration can be repeated periodically, e.g., hourly, daily, weekly, biweekly (i.e., every two weeks), for one, two, three, four, or more months. After an initial treatment regimen, treatment can be administered less frequently. For example, after three months of biweekly administration, administration can be repeated once per month for six months or more than one year. C5 inhibitor administration may decrease, reduce, increase, or alter binding or any physiologically deleterious process (e.g., in the patient's cells, tissues, blood, urine, or other parts) by at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, or at least 90% or more.

[0216] Intravenously delivered C5 inhibitory cyclic polypeptides (e.g., zilucoplan and / or its active metabolites or variants) can be delivered by infusion over a period of time, such as over a period of 5, 10, 15, 20, or 25 minutes. Administration can be repeated periodically, for example, hourly, daily, weekly, biweekly (i.e., every two weeks), for one, two, three, four, or more months. After an initial treatment regimen, treatment can be administered less frequently. For example, after three months of biweekly administration, administration can be repeated once a month for six months or more than one year. Administration of a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or its active metabolite or variant) may decrease, reduce, increase, or alter binding or any physiologically deleterious process (e.g., in a patient's cells, tissues, blood, urine, or other parts) by at least 10%, at least 15%, at least 20%, at least 25%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, or at least 90% or more.

[0217] Prior to administration of the full amount of a C5 inhibitor described herein (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or an active metabolite or variant thereof) and / or composition thereof, the patient can be administered a lower dose, such as 5% of the full dose, and monitored for adverse effects, such as allergic or infusion reactions, or for elevated lipid levels or blood pressure. In another example, the patient can be monitored for unwanted immunostimulatory effects, such as increased cytokine (e.g., TNF-alpha, IL-1, IL-6, or IL-10) levels.

[0218] Genetic predisposition plays a role in the development of some diseases or disorders. Thus, patients in need of a C5 inhibitor (e.g., a C5 inhibitor polypeptide, a C5 inhibitor cyclic polypeptide, zilucoplan, and / or its active metabolites or variants) can be identified by family history analysis or screening for, for example, one or more genetic markers or variants. A healthcare provider (e.g., a doctor or nurse) or a relative can analyze family history information before prescribing or administering a therapeutic composition of the present disclosure.

[0219] III. Kits and Devices In some embodiments, the present disclosure provides kits and devices. Such kits and devices may include any of the compounds (e.g., therapeutic agents, C5 inhibitors, C5 inhibitor polypeptides, C5 inhibitory cyclic polypeptides, zilucoplan, and / or active metabolites or variants thereof) and / or compositions thereof described herein. Such kits and devices may include a C5 inhibitory cyclic polypeptide (e.g., zilucoplan and / or active metabolites or variants thereof) or composition described herein. In a non-limiting example, zilucoplan and / or compositions thereof may be included. Such kits may be used to practice the methods of treating complement-related indications described herein.

[0220] Kit components may be packaged in liquid (e.g., aqueous or organic) media or in dry (e.g., lyophilized) form. Kits may include containers, including, but not limited to, vials, test tubes, flasks, bottles, syringes, or bags. Kit containers can be used to subdivide, preserve, store, isolate, and / or protect kit components. Kit components may be packaged together or separately. Some kits may include containers of sterile, pharmaceutically acceptable buffers and / or other diluents (e.g., phosphate-buffered saline). In some embodiments, kits include containers of kit components in dry form, along with another container of a solution for dissolving the dried components. In some embodiments, kits include a syringe for administering one or more kit components.

[0221] When the polypeptide is provided as a dry powder, it is contemplated that 10 micrograms to 1000 milligrams of polypeptide, or at least that amount, or at most that amount, will be provided in the kit.

[0222] The container may include at least one vial, test tube, flask, bottle, syringe, and / or other receptacle into which the polypeptide formulation may be placed, and preferably suitably dispensed. The kit may also include containers for sterile, pharmaceutically acceptable buffers and / or other diluents.

[0223] The kit may include instructions for utilizing the kit components as well as the use of any other reagents not included in the kit. The instructions may include executable variations. In some embodiments, the present disclosure provides a kit including a syringe containing Zilcoplan and instructions. The syringe may be an autoinjector. The autoinjector may include a BD ULTRASAFE PLUS™ self-administration device (Becton Dickinson (BD), Franklin Lakes, New Jersey). The kit may include one or more items for treating syringe wounds. Such items may include, but are not limited to, alcohol wipes and wound dressings (e.g., cotton balls, mesh pads, bandages, tape, gauze, etc.). The kit may further include a disposal container for disposal of used kit components. The disposal container may be designed for disposal of sharp objects, such as needles and syringes. Some kits may include instructions for disposal of sharp objects.

[0224] In some embodiments, the kits of the present disclosure include zilcoplan in powder form or in a dissolved state. The solution may be an aqueous solution. The solution may include PBS. The zilcoplan solution may include about 4 mg / ml to about 200 mg / ml zilcoplan. In some embodiments, the zilcoplan solution includes about 40 mg / ml zilcoplan. The zilcoplan solution may include a preservative. In some embodiments, the zilcoplan solution is preservative-free.

[0225] IV. Definition Administered in Combination: As used herein, the term "administered in combination" or "co-administration" refers to simultaneous exposure to two or more agents, either simultaneously or within a time interval such that a subject is simultaneously exposed to both at some point in time and / or administered within such a time interval that there may be overlap in the effects of each agent on the patient. In some embodiments, at least one dose of one or more agents is administered within about 24 hours, 12 hours, 6 hours, 3 hours, 1 hour, 30 minutes, 15 minutes, 10 minutes, 5 minutes, or 1 minute of at least one administration of one or more other agents. In some embodiments, administration is in an overlapping dosing regimen. As used herein, the term "dosing regimen" refers to multiple doses separated by time intervals. Such administration may be at regular intervals or may include one or more breaks in administration. Bioavailability: As used herein, the term "bioavailability" refers to the systemic availability of a given amount of a compound (e.g., a C5 inhibitor) administered to a subject. Bioavailability can be measured as the area under the curve (AUC) or maximum serum or plasma concentration (C) of the unchanged form of a compound following administration of the compound to a subject. max AUC can be calculated by measuring the area under the curve (AUC). AUC is a determination of the area under the curve when the serum or plasma concentration of a compound is plotted on the ordinate (Y-axis) against time on the abscissa (X-axis). Generally, the AUC for a particular compound can be calculated using methods known to those of skill in the art and / or as described in GS Banker, Modern Pharmaceutics, Drugs and the Pharmaceutical Sciences, Vol. 72, Marcel Dekker, New York, Inc., 1996, the contents of which are incorporated herein by reference in their entirety.

[0226] Biological system: As used herein, the term "biological system" refers to a cell, a group of cells, a tissue, an organ, a group of organs, an organelle, a body fluid, a biological signaling pathway (e.g., a receptor-activated signaling pathway, a charge-activated signaling pathway, a metabolic pathway, a cell signaling pathway, etc.), a group of proteins, a group of nucleic acids, or a group of molecules (including, but not limited to, biomolecules) that perform at least one biological function or role within a cell membrane, a subcellular compartment, a cell, a cell culture, a tissue, an organ, an organ system, an organism, a multicellular organism, a body fluid, or any biological entity. In some embodiments, the biological system is a cell signaling pathway that includes intracellular and / or extracellular signaling biomolecules. In some embodiments, the biological system includes a proteolytic cascade (e.g., the complement cascade).

[0227] Buffering Agent: As used herein, the term "buffering agent" refers to a compound used in a solution to resist changes in pH. Such compounds may include, but are not limited to, acetic acid, adipic acid, sodium acetate, benzoic acid, citric acid, sodium benzoate, maleic acid, sodium phosphate, tartaric acid, lactic acid, potassium metaphosphate, glycine, sodium bicarbonate, potassium phosphate, sodium citrate, and sodium tartrate.

[0228] Clearance rate: As used herein, the term "clearance rate" refers to the rate at which a particular compound is removed from a biological system or fluid. Compound: As used herein, the term "compound" refers to an individual chemical compound. In some embodiments, a particular compound may exist in one or more isomeric or isotopic forms (including, but not limited to, stereoisomers, geometric isomers, and isotopes). In some embodiments, a compound is provided or utilized in only one such form. In some embodiments, a compound is provided or utilized as a mixture of two or more such forms (including, but not limited to, a racemic mixture of stereoisomers). One of ordinary skill in the art will recognize that some compounds exist in different forms and exhibit different properties and / or activity (including, but not limited to, biological activity). In such cases, it is within the ordinary skill of one of ordinary skill in the art to select or avoid a particular form of a compound for use in accordance with the present disclosure. For example, compounds containing asymmetrically substituted carbon atoms can be isolated in optically active or racemic form.

[0229] Cyclic or Cyclized: As used herein, the term "cyclic" refers to the presence of a continuous loop. A continuous loop can be formed by a chemical bond between different regions of a compound (also referred to herein as a "cyclic bond"). A cyclic molecule need not be circular, it need only be joined to form an unbroken chain of subunits. A cyclic polypeptide can contain a "cyclic loop" formed when two amino acids are joined by a bridging moiety. The cyclic loop includes amino acids along the polypeptide that lie between the bridged amino acids. A cyclic loop can contain 2, 3, 4, 5, 6, 7, 8, 9, 10, or more amino acids.

[0230] Downstream Event: As used herein, the term "downstream" or "downstream event" refers to any event that occurs after and / or as a result of another event. In some cases, a downstream event is an event that occurs after and as a result of C5 cleavage and / or complement activation. Such events can include, but are not limited to, the generation of C5 cleavage products, activation of MAC, hemolysis, and hemolysis-related diseases (e.g., PNH).

[0231] Equilibrium dissociation constant: As used herein, the term "equilibrium dissociation constant" or "KD " refers to a value that represents the tendency of two or more agents (e.g., two proteins) to reversibly separate. In some cases, K D indicates the concentration of the primary agent at which half of the total level of the secondary agent is associated with the primary agent.

[0232] Half-life: As used herein, the term "half-life" or "t 1 / 2 "Terminal half-life" or "terminal t" refers to the time it takes for a given process or compound concentration to reach half of its final value. 1 / 2 " refers to the time required for the plasma concentration of a factor to decrease by half after the factor's concentration has reached pseudo-equilibrium.

[0233] Identity: As used herein, the term "identity," when referring to polypeptides or nucleic acids, refers to the relative relationship between sequences. The term is used to describe the degree of sequence similarity between polymer sequences and can include the percentage of matching monomer components, with gap alignment (if present) considered by a particular mathematical model or computer program (i.e., "algorithm"). The identity of related polypeptides can be readily calculated by known methods. Such methods include those previously described by others (Lesk, AM, ed., Computational Molecular Biology, Oxford University Press, New York, 1988; Smith, DW, ed., Biocomputing: Informatics and Genome Projects, Academic Press, New York, 1993; Griffin, AM et al., eds., Computer Analysis of Sequence Data, Part 1, Humana Press, New Jersey, 1994; von Heinje, G., Sequence Analysis in Molecular Biology, 1995; Biology, Academic Press, 1987; Gribskov, M. et al. (eds.), Sequence Analysis Primers and Carillo et al., Applied Mathematics, Society for Industrial and Applied Mathematics Journal (SIAM J), 1988, Vol. 48, p. 1073.

[0234] Inhibitor: As used herein, the term "inhibitor" refers to any agent that blocks or reduces the occurrence of a particular event; cell signal; chemical pathway; enzymatic reaction; cellular process; interaction between two or more entities; biological event; disease; disorder; or pathological condition.

[0235] Loading dose: As used herein, an "initial loading dose" refers to an initial dose of a therapeutic agent, which may be different from one or more subsequent doses. A loading dose may be used to achieve an initial concentration or level of activity of a therapeutic agent before subsequent doses are administered.

[0236] Intravenous: As used herein, the term "intravenous" refers to the area within a blood vessel. Intravenous administration typically refers to the delivery of a compound into the blood by injection into a blood vessel (e.g., a vein). In vitro: As used herein, the term "in vitro" refers to events that take place in an artificial environment (e.g., in a test tube or reaction vessel, in cell culture, in a Petri dish, etc.) rather than in a living organism (e.g., an animal, plant, or microorganism).

[0237] In vivo: As used herein, the term "in vivo" refers to events that take place within an organism (e.g., an animal, plant, or microorganism, or its cells or tissues). Lactam bridge: As used herein, the term "lactam bridge" refers to an amide bond that forms a bridge between chemical groups in a molecule. In some cases, lactam bridges are formed between amino acids in a polypeptide.

[0238] Linker: As used herein, the term "linker" refers to a group of atoms (e.g., 10-1,000 atoms), molecule, or other compound used to link two or more entities. A linker can bind such entities through covalent or non-covalent (e.g., ionic or hydrophobic) interactions. A linker can include a chain of two or more polyethylene glycol (PEG) units. In some cases, a linker can be cleavable.

[0239] Minute ventilation: As used herein, the term "minute ventilation" refers to the volume of air inspired or exhaled from a subject's lungs per minute. Non-proteinogenic: As used herein, the term "non-proteinogenic" refers to any non-naturally occurring protein, including those with non-naturally occurring components, such as non-naturally occurring amino acids.

[0240] Patient: As used herein, "patient" refers to a subject who may be seeking or in need of treatment, who requests treatment, is undergoing treatment, will receive treatment, or who is receiving the care of a trained professional for a particular disease or condition.

[0241] Pharmaceutical composition: As used herein, the term "pharmaceutical composition" refers to a composition having at least one active ingredient (e.g., a C5 inhibitor) in a form and in an amount that makes the active ingredient therapeutically effective.

[0242] Pharmaceutically acceptable: The phrase "pharmaceutically acceptable" is used herein to refer to compounds, materials, compositions, and / or dosage forms that are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication commensurate with a reasonable benefit / risk ratio.

[0243] Pharmaceutically acceptable excipient: As used herein, the phrase "pharmaceutically acceptable excipient" refers to any component, other than the active agent (e.g., the active agent zilucoplan and / or its active metabolite or variant thereof), present in a pharmaceutical composition that is substantially non-toxic and non-inflammatory in a patient. In some embodiments, the pharmaceutically acceptable excipient is a vehicle capable of suspending or dissolving the active agent. Excipients may include, for example: anti-adherents, antioxidants, binders, coatings, compression aids, disintegrants, dyes (colorants), softeners, emulsifiers, fillers (diluents), film-forming agents or coatings, flavors, fragrances, glidants (flow enhancers), lubricants, preservatives, printing inks, adsorbents, suspending or dispersing agents, sweeteners, and water of hydration. Exemplary excipients include, but are not limited to, butylated hydroxytoluene (BHT), calcium carbonate, calcium phosphate (dibasic), calcium stearate, croscarmellose, cross-linked polyvinylpyrrolidone, citric acid, crospovidone, cysteine, ethylcellulose, gelatin, hydroxypropyl cellulose, hydroxypropylmethylcellulose, lactose, magnesium stearate, maltitol, mannitol, methionine, methylcellulose, methylparaben, microcrystalline cellulose, polyethylene glycol, polyvinylpyrrolidone, povidone, pregelatinized starch, propylparaben, retinyl palmitate, shellac, silicon dioxide, sodium carboxymethylcellulose, sodium citrate, sodium starch glycolate, sorbitol, starch (corn), stearic acid, sucrose, talc, titanium dioxide, vitamin A, vitamin E, vitamin C, and xylitol.

[0244] Plasma Compartment: As used herein, the term "plasma compartment" refers to the intravascular space occupied by plasma. Salt: As used herein, the term "salt" refers to a compound made up of a cation and an associated anion. Such compounds may include sodium chloride (NaCl) or other types of salts, including, but not limited to, acetates, chlorides, carbonates, cyanides, nitrites, nitrates, sulfates, and phosphates. The term "salt" may also be used to refer to salt forms of the polypeptides described herein (e.g., zilcoplan salts). Such polypeptide salts may include zilcoplan sodium salt.

[0245] Sample: As used herein, the term "sample" refers to an aliquot or portion taken from a source and / or provided for analysis or processing. In some embodiments, a sample is derived from a biological source, such as a tissue, cell, or component (e.g., a bodily fluid, including, but not limited to, blood, mucus, lymph, synovial fluid, cerebrospinal fluid, saliva, amniotic fluid, amniotic cord blood, urine, vaginal fluid, and semen). In some embodiments, a sample can be or include a homogenate, lysate, or extract prepared from a whole organism or a subset of its tissues, cells, or components, or a part or portion thereof, including, but not limited to, plasma, serum, spinal fluid, lymph, an external strip of skin, the respiratory, intestinal, and genitourinary tracts, tears, saliva, milk, blood cells, a tumor, or an organ. In some embodiments, a sample is or includes a medium, such as a nutrient broth or gel, which may contain cellular components, such as proteins. In some embodiments, a "primary" sample is an aliquot of a source. In some embodiments, the primary sample is subjected to one or more processing (eg, separation, purification, etc.) steps to prepare the sample for analysis or other use.

[0246] Subcutaneous: As used herein, the term "subcutaneous" refers to the space below the skin. Subcutaneous administration is the delivery of a compound below the skin. Subject: As used herein, the term "subject" refers to any living organism to which a compound or method according to the present disclosure can be administered or applied, e.g., for experimental, diagnostic, prophylactic, and / or therapeutic purposes. Typical subjects include animals (e.g., mammals such as mice, rats, rabbits, porcine subjects, non-human primates, and humans).

[0247] Substantially: As used herein, the term "substantially" refers to a qualitative condition indicating the total or near total extent or degree of the characteristic or property in question. Those skilled in the art of biology will understand that biological and chemical phenomena rarely, if ever, proceed to completion and / or perfection, or achieve or avoid absolute results. Thus, the term "substantially" is used herein to capture the potential lack of perfection inherent in many biological and chemical phenomena.

[0248] Therapeutically effective amount: As used herein, the term "therapeutically effective amount" refers to the amount of an agent (e.g., a C5 inhibitor) delivered that, when administered to a subject suffering from or susceptible to a disease, disorder, and / or condition, is sufficient to treat, ameliorate the symptoms of, diagnose, prevent, and / or delay the onset of the disease, disorder, and / or condition.

[0249] Tidal Volume: As used herein, the term "tidal volume" refers to the normal lung volume of air expelled during breathing (without special effort). T max As used herein, the term "T max " refers to the period of time during which the maximum concentration of a compound in a subject or fluid is maintained.

[0250] Treating: As used herein, the term "treating" refers to partially or completely alleviating, ameliorating, improving, relieving, delaying the onset of, inhibiting the progression of, reducing the severity of, and / or reducing the incidence of one or more symptoms or characteristics of a particular disease, disorder, and / or condition. Treatment may be administered to subjects who do not show signs of the disease, disorder, and / or condition and / or to subjects who show only early signs of the disease, disorder, and / or condition, for the purpose of reducing the risk of developing conditions associated with the disease, disorder, and / or condition.

[0251] Therapeutic Dose: As used herein, a "therapeutic dose" refers to one or more doses of a therapeutic agent administered in the course of addressing or alleviating a therapeutic indication. A therapeutic dose can be adjusted to maintain a desired concentration or activity level of the therapeutic agent in a bodily fluid or biological system.

[0252] Volume of distribution: As used herein, the term “volume of distribution” or “V dist " refers to the volume of fluid required to contain the entire amount of a compound in the body at the same concentration as in blood or plasma. The volume of distribution may reflect the extent to which a compound is present in extravascular tissues. A large volume of distribution reflects the tendency of a compound to bind to tissue components relative to plasma protein components. In a clinical situation, V dist can be used to determine a loading dose of a compound to achieve a steady state concentration of that compound.

[0253] V. Equivalence and Scope While various embodiments of the present invention have been shown and described in detail, it will be understood by those skilled in the art that various changes in form or detail can be made therein without departing from the spirit and scope of the invention as defined by the appended claims.

[0254] Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments in accordance with the invention described herein. The scope of the present invention is not limited by the above description, but is instead set forth in the appended claims.

[0255] In the claims, articles such as "a," "an," and "the" can mean one or more, unless indicated otherwise or clear from the context. A claim or description including "or" between one or more members of a group is considered to be satisfied when one, more than one, or all of the group members are present in, employed in, or otherwise relevant to a given product or process, unless indicated otherwise or clear from the context. The invention includes embodiments in which exactly one member of a group is present in, employed in, or otherwise relevant to a given product or process. The invention includes embodiments in which two or more or all group members are present in, employed in, or otherwise relevant to a given product or process.

[0256] It is also noted that the term "comprising" is intended to be open-ended, allowing but not requiring the inclusion of additional elements or steps. When the term "comprising" is used herein, the terms "consisting of" and "or including" are also included and disclosed.

[0257] Where ranges are given, endpoints are included. Furthermore, unless otherwise stated or apparent from the context and the understanding of one of ordinary skill in the art, it should be understood that values expressed as ranges can encompass every specific value or subrange within the stated range in different embodiments of the invention, down to one-tenth of the unit of the lower limit of that range, unless the context clearly dictates otherwise.

[0258] Furthermore, it should be understood that any particular embodiment of the present invention that is within the prior art may be expressly excluded from any one or more of the claims. Because such embodiments are deemed to be known to those of skill in the art, they may be excluded even if the exclusion is not expressly stated herein. Any particular embodiment of the compositions of the present invention (e.g., any nucleic acid or protein encoded thereby; any method of production; any method of use; etc.) may be excluded from any one or more of the claims for any reason, whether or not related to the existence of prior art.

[0259] All cited sources, e.g., references, publications, databases, database entries, and art cited therein, are incorporated herein by reference, even if not expressly stated in the citation. In the event of a conflict between statements in a cited source and this application, the statements in this application shall control.

[0260] Section and table headings are not intended to be limiting. [Example]

[0261] Example 1. Formation and testing of PLGA particles Studies were conducted to develop zilcoplan-loaded PLGA microsphere particles for drug delivery. Several parameters for particle formation were manipulated to optimize zilcoplan delivery characteristics. Initial studies utilized both single and double PLGA emulsion formats. Resomer® 502H (Evonik, Germany), an acid-terminated formulation with a MW of 7,000 to 17,000 and a degradation time of less than 3 months, was used with different zilcoplan loading percentages.

[0262] Zircoplan (SEQ ID NO: 1), described in WO 2017105939 and WO 2018106859, was prepared as a cyclic peptide containing 15 amino acids (four of which are unnatural amino acids), an acetylated N-terminus, and a C-terminal carboxylic acid. The C-terminal lysine of the core peptide has a modified side chain to form an N-ε-(PEG24-γ-glutamic acid-N-α-hexadecanoyl) lysine residue. This modified side chain contains a polyethylene glycol spacer (PEG24) attached to an L-γ-glutamic acid residue derivatized with a palmitoyl group. Cyclization of zircoplan is via a lactam bridge between the side chains of L-Lys1 and L-Asp6. All amino acids in zircoplan are L-amino acids. Zircoplan has a molecular weight of 3562.23 g / mol and a C 172 H 278 N 24 O55 It has the chemical formula:

[0263] PLGA formulation Zircoplan was incorporated into poly(lactic-co-glycolic acid) (PLGA) particles by emulsification using either a single emulsion (oil-in-water) or a double emulsion (water-in-oil-in-water) format. Typically, PLGA droplets in an organic solvent (dichloromethane) were prepared at a ratio of 1 g of PLGA per 10 mL of organic solvent. The droplets were emulsified in an aqueous continuous phase in the presence of an emulsifier (polyvinyl alcohol (PVA)) and zircoplan. The resulting emulsion was treated to evaporate the organic solvent, forming condensed zircoplan-PLGA particles. Batches were prepared using either rapid evaporation (the organic solvent appears in the solution as it is withdrawn) or rotary evaporation (rotavap) methods. Morphological changes were observed in particles prepared by rotavap, such as collapsed or concave spherical structures when observed by electron microscopy.

[0264] Furthermore, different pore-forming excipients (PFEs) were explored in the particle formulation to enhance the release of zilcoplan. These included 10% medium-chain triglycerides (MCTs), Pluronic® F-127 (BASF, Florham Park, NJ), or poly(ethylene glycol) MW3400 (PEG3400). Ultimately, PFEs were omitted because it was found that high-zilcoplan-loaded formulations provided good drug release without PFEs.

[0265] The double emulsion formulation showed an initial burst of 12.5% at a zilcoplan loading of 29%, which more than doubled when the zilcoplan loading was increased to 32%. The initial single emulsion formulation at a low zilcoplan loading percentage (11.24%) showed a low initial burst percentage (5.6%). By adjusting the process to 1 gram, an even lower initial burst (5%) was obtained at a higher zilcoplan loading percentage (14%). By omitting DMSO from the formulation, an initial burst of less than 5% was achieved at a zilcoplan loading percentage of 34.3%.

[0266] Single emulsion formulations with zircoplan loading percentages of 36-37.5% had the highest tolerable loading before burst values became excessive (presumably due to the level of surface-associated zircoplan). These highly loaded formulations were selected for further analysis. Quenched and rotavap processed forms were tested. Uniform zircoplan distribution along with particle uniformity was confirmed using scanning electron microscopy and energy dispersive X-ray spectroscopy, respectively. Particles were generally spherical with little internal void. Elemental mapping of zircoplan-Na+ showed an overall uniform distribution.

[0267] Animal testing Zilcoplan PLGA formulations with a 37% zilcoplan load, prepared by quenching or rotavap processing, were administered to rats and compared with a formulation with a 22% zilcoplan load. The formulations were administered to rats by subcutaneous injection, and zilcoplan levels were determined by mass spectrometry in rat plasma samples obtained at various time points after administration. Zilcoplan levels were higher in samples obtained through week 1 from rats receiving the higher-loaded formulation (see Figure 1). Particles prepared by quenching showed lower initial burst levels, but by 48 hours after administration, higher levels were observed in samples that persisted through week 1.

[0268] A similar study was conducted in non-human primates (NHPs), but the zilcoplan loading in the highly loaded formulation was 36%. The formulations were administered to cynomolgus monkeys at a fixed dose of 8 mg / kg. As in the rat study, a higher initial burst was observed with the higher zilcoplan loading percentage formulation (see Figure 2). The observed burst was useful for exceeding the 95% effective concentration (EC95) of 8,000 ng / mL within the first few days. By day 17 after administration, the 22% zilcoplan loaded formulation had a 4,359,795 ng * h / mL, whereas the higher-load quench formulation produced an area under the curve (AUC) of 5,141,124 mg / mL. *h / mL, and the higher-load rotavap formulation produced an AUC of 5,389,580 ng * AUC in h / mL was generated.

[0269] The same study was repeated at different doses using a 36% zilucoplan-loaded formulation prepared by rapid cooling. Doses of 4, 8, and 16 mg / kg were tested to assess the dose-exposure relationship. A clear dose-exposure relationship was demonstrated at early time points up to 4 weeks post-dose (see Figure 3). 6,417,235 ng at the 4 mg / kg dose. * h / mL, yielding an AUC of 7,865,963 ng at an 8 mg / kg dose. * h / mL, and a dose of 16 mg / kg produced an AUC of 11,375,456 ng * A comparison of the results from the 8 mg / kg dose with those from the previous study revealed a similar AUC (5,276,571 ng / mL) at 17 days post-treatment. * h / mL vs. 5,141,124 ng * h / mL) and the maximum concentration (C max ) (18,476 ng / mL vs. 18,558 ng / mL).

[0270] Percent hemolysis associated with plasma samples was measured for samples obtained at multiple time points following subcutaneous administration of zilucoplan-PLGA (a formulation with a 36% zilucoplan load prepared using a rapid cooling process) in NHPs. Cynomolgus monkeys received an initial loading dose of 16 mg / kg zilucoplan-PLGA on day 1, followed by 10 mg / kg doses on days 8 and 15. Levels of hemolysis greater than 90% were maintained throughout the week following the initial dose. After a second dose on day 8, hemolysis levels further decreased. By the end of the second week, hemolysis levels had decreased (<95%) to levels consistent with those observed in humans receiving daily subcutaneous administration of a non-sustained-release formulation (zilucoplan at a dose of 0.3 mg / kg formulated at 40 mg / mL in a buffer with 50 mM sodium phosphate and 75.7 mM sodium chloride at pH 7.0) within the same time frame.

[0271] Example 2. Prediction of human administration Properties from a zilucoplan-PLGA formulation (36% zilucoplan loading via quenching) tested in NHPs were used to predict appropriate dosing for human trials using a human PK model. The model utilized input properties based on deconvolution of NHP study data and assumed 75 kg human subjects receiving weekly and biweekly dosing until steady state. Based on the model, predicted dose ranges were between 100 mg and 200 mg for weekly dosing in humans and between 200 mg and 300 mg for biweekly dosing.

[0272] A 100 mg weekly dose of zilucoplan-PLGA was predicted to produce daily zilucoplan plasma concentrations equivalent to those of a 0.3 mg / kg daily subcutaneous formulation (40 mg / mL solution with 50 mM sodium phosphate and 75.7 mM sodium chloride at a pH of 7.0), resulting in an approximately 35% reduction in the amount of zilucoplan administered compared to daily dosing. Weekly dosing was predicted to have a narrow range between the minimum concentration (Cmin) and Cmax. Without a loading regimen, weekly dosing was predicted to reach effective plasma concentrations (5,000 ng / mL) within 10 days. A 200 mg biweekly dose of zilucoplan-PLGA was predicted to maintain effective drug concentrations with plasma concentration equivalent to 0.3 mg / kg for 10 out of 14 days. Overall, the zilucoplan-PLGA formulation was predicted to achieve approximately 33% dosing efficiency compared to a 7-day or 14-day dose of the standard immediate-release formulation.

Claims

1. Zilcoplan, a C5-inhibiting cyclic polypeptide comprising the amino acid sequence of SEQ ID NO: 1, or a salt thereof; and 1. A modified release matrix comprising a polymer, the polymer comprising polylactic acid-co-glycolic acid (PLGA) comprising polylactic acid and polyglycolic acid in a ratio of 25:75 to 75:

25. A sustained-release formulation comprising:

2. The sustained-release formulation of claim 1, wherein the PLGA has a ratio of polylactic acid to polyglycolic acid of 50:

50.

3. A sustained-release formulation as described in claim 1 or 2, wherein the release-controlling matrix comprises an emulsion.

4. The sustained-release formulation of claim 3, wherein the emulsion comprises a single emulsion or a double emulsion.

5. A sustained-release formulation described in any one of claims 1 to 4, which contains an excipient.

6. The sustained-release formulation of claim 5, wherein the excipient comprises a pore-forming excipient (PFE).

7. The sustained-release formulation of claim 6, wherein the PFE is selected from the group consisting of medium-chain triglycerides, Pluronic® F-127, and poly(ethylene glycol) (PEG).

8. A sustained-release formulation according to any one of claims 1 to 7, wherein the release-modifying matrix comprises particles having a diameter of 5 μm to 200 μm.

9. The sustained-release formulation of claim 1, wherein the polypeptide comprises a PEG moiety.

10. The sustained-release formulation of claim 9, comprising zilucoplan at a concentration of 1 mg / mL to 400 mg / mL.

11. A sustained-release formulation described in any one of claims 1 to 10, comprising 10% to 95% by weight of the release-modifying matrix.

12. A sustained-release formulation according to any one of claims 1 to 11, wherein the polypeptide is uniformly distributed in the release-controlling matrix.

13. A method for preparing the sustained-release formulation according to any one of claims 1 to 12, comprising: preparing an organic phase solution, the organic phase solution being prepared by mixing an organic solvent, PLGA, and the polypeptide; preparing an aqueous phase solution, the aqueous phase solution being prepared by mixing an aqueous solution with an emulsion stabilizer; preparing the sustained release formulation by preparing an emulsion of the organic phase solution and the aqueous phase solution; A method comprising:

14. The method of claim 13, wherein the organic solvent comprises dichloromethane (DCM).

15. The method of claim 13 or 14, wherein the emulsion stabilizer comprises polyvinyl alcohol (PVA).

16. A method described in any one of claims 13 to 15, wherein the polypeptide is mixed in the organic phase solution at a concentration sufficient to obtain 10% to 50% by weight of the polypeptide in the sustained release formulation.

17. The sustained-release formulation has sustained-release properties, The sustained release characteristics include a low initial burst in the release of the polypeptide and / or the ability to obtain an effective concentration of the polypeptide in a medium in which the polypeptide is released from the sustained release formulation. The sustained release formulation according to any one of claims 1 to 12.

18. The sustained-release formulation of claim 17, wherein the ability to obtain the effective concentration of the polypeptide in the medium in which the polypeptide is released from the sustained-release formulation persists for a specific period of time.

19. The sustained-release formulation of claim 18, wherein the specific period is 1 week to 3 weeks.

20. A sustained-release formulation described in any one of claims 17 to 19, wherein the effective concentration is 4,000 ng / mL to 12,000 ng / mL.

21. A sustained-release formulation described in any one of claims 17 to 20, wherein the initial burst in the release of the polypeptide is 0% to 20% of the total amount of the polypeptide contained in the sustained-release formulation.

22. The sustained-release formulation of claim 21, wherein the initial burst is less than 5%.

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