Heteromultimers that bind to DLL3 and CD3

Abstract

The present disclosure provides a heteromultimer comprising a first heterodimer that binds to human delta-like ligand 3 (DLL3) and a second heterodimer that binds to human CD3, which can bind to DLL3-expressing cancer cells. The present disclosure also provides a method of treating a DLL3-expressing cancer in a subject in need thereof, comprising administering to the subject an effective amount of a heteromultimer or a composition comprising the heteromultimer. The present disclosure provides a heteromultimer, wherein: (a) the first heterodimer comprises a heavy chain (HC) comprising the amino acid sequence of SEQ ID NO:54 or SEQ ID NO:58; and a light chain (LC) comprising the amino acid sequence of SEQ ID NO:55 or SEQ ID NO:59; (b) the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:56 or SEQ ID NO:132; and a light chain comprising the amino acid sequence of SEQ ID NO:57.

Description

[Technical field]

[0001] The present disclosure relates to multimeric antigen binding proteins that bind to DLL3 and CD3.

[0002] INCORPORATION BY REFERENCE OF MATERIAL SUBMITTED ELECTRONICALLY The present specification incorporates by reference in its entirety the nucleotide / amino acid sequence listing, which was submitted contemporaneously herewith and is identified as follows: One XML document of 90.8 kilobytes entitled "10092-WO01-SEC.xml", created on April 25, 2023.

[0003] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Patent Application No. 63 / 338,751, filed May 5, 2022. [Background technology]

[0004] Small cell lung cancer (SCLC) is an aggressive form of lung cancer with a poor prognosis and limited treatment options, accounting for approximately 13% of all newly diagnosed lung cancers, with over 235,000 adults receiving a diagnosis of SCLC in the United States in 2021. Survival rates have remained low for decades, with only 5% of patients with SCLC surviving 7 years, largely due to the lack of new treatments to combat this form of lung cancer. Most patients present with extensive stage disease, but approximately one-third of patients present with limited stage disease, defined as tumor in only one breast and contained within a single radiation field. Disseminated metastatic tumors with lymphoma-like features are a hallmark of SCLC. The first known diagnosis of a patient with SCLC described it as a disease of the lymphatic system, and SCLC was not recognized as a lung cancer until 1926, highlighting the unique nature of SCLC tumors compared to other solid tumors.

[0005] Patients typically respond well to current standard treatments, including chemotherapy combined with thoracic radiation therapy (TRT), but invariably relapse with chemotherapy-resistant disease for which there are currently no available treatment options. Recently, the addition of the anti-PD-L1 antibody atezolizumab (TECENTRIQ®) to carboplatin and etoposide chemotherapy has demonstrated improved overall survival (OS) in first-line therapy, which led to the approval of this regimen by the United States Food and Drug Administration (FDA) for the first-line treatment of advanced-stage SCLC. Despite these treatment advances, the prognosis in the relapsed refractory (RR) setting remains very poor, with rapid disease progression and short median survival of less than 6 months. In addition, patients with SCLC have a high incidence of comorbidities, including hypertension, heart disease, diabetes, and paraneoplastic syndromes. These, combined with the typical advanced age of SCLC patients, affect the patient's ability to tolerate demanding chemotherapy regimens, further limiting treatment options.

[0006] Delta-like ligand 3 (DLL3) is an inhibitory Notch ligand that is highly expressed in SCLC and other neuroendocrine tumors, but minimally expressed in normal tissues. In one study, approximately 86% of analyzed SCLC tumors showed evidence of DLL3 expression by RNA-seq (Giffin et al., Clin. Cancer Res., 27(5):1526-1537(2021).doi:10.1158 / 1078-0432.CCR-20-2845). In contrast, only a few normal cell types have been shown to express DLL3 (e.g., neurons, pancreatic islet cells, and pituitary cells), and such expression was primarily cytoplasmic. Recent studies have reported that DLL3 is also expressed in other tumor types of neuroendocrine origin, including melanoma, glioblastoma multiforme, neuroendocrine prostate cancer (NEPC), and large cell neuroendocrine lung tumors (Giffin et al., Clin. Cancer Res., 27(5):1526-1537 (2021) and Saunders et al., Sci Transl Med., 7(302):302ra136. doi:10.1126 / scitranslmed.aac9459 (2015)). There remains a need for compositions and methods that more effectively target and treat neuroendocrine cancers, including but not limited to small cell lung cancer. [Prior art documents] [Non-patent literature]

[0007] [Non-Patent Document 1] Giffin et al., Clin. Cancer Res., 27(5):1526-1537(2021). [Non-Patent Document 2] Saunders et al., Sci Transl Med., 7(302):302ra136. Summary of the Invention [Means for solving the problem]

[0008] The present disclosure provides a heteromultimer comprising a first heterodimer that binds to human delta-like ligand 3 (DLL3) and a second heterodimer that binds to human cluster of differentiation (CD) 3, wherein: (a) the first heterodimer comprises a heavy chain (HC) comprising the amino acid sequence of SEQ ID NO:54 or SEQ ID NO:58; and a light chain (LC) comprising the amino acid sequence of SEQ ID NO:55 or SEQ ID NO:59; and (b) the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:56 or SEQ ID NO:132; and a light chain comprising the amino acid sequence of SEQ ID NO:57.

[0009] In some embodiments, (a) the first heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 54 and a light chain comprising the amino acid sequence of SEQ ID NO: 55; (b) the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 56 and a light chain comprising the amino acid sequence of SEQ ID NO: 57.

[0010] In some embodiments, (a) the first heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 54 and a light chain comprising the amino acid sequence of SEQ ID NO: 55; and (b) the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 132 and a light chain comprising the amino acid sequence of SEQ ID NO: 57.

[0011] In some embodiments, (a) the first heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:58 and a light chain comprising the amino acid sequence of SEQ ID NO:59; and (b) the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:56 and a light chain comprising the amino acid sequence of SEQ ID NO:57.

[0012] In some embodiments, (a) the first heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:58 and a light chain comprising the amino acid sequence of SEQ ID NO:59; and (b) the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:132 and a light chain comprising the amino acid sequence of SEQ ID NO:57.

[0013] The present disclosure also provides a composition comprising the heteromultimer described above and a pharma- ceutically acceptable carrier. In some embodiments, the composition comprises the heteromultimer described above for use in a method for treating a DLL3-expressing cancer, such as a neuroendocrine cancer (e.g., small cell lung cancer (SCLC), neuroendocrine prostate cancer (NEPC), or neuroblastoma).

[0014] Kits containing the above compositions and instructions for use are also provided.

[0015] The present disclosure provides a method of inhibiting the proliferation of DLL3-expressing cancer cells, comprising contacting a population of DLL3-expressing cancer cells and CD3-expressing T cells with an effective amount of the heteromultimer or composition described above.

[0016] The present disclosure further provides a method of treating a DLL3-expressing cancer in a subject in need thereof, comprising administering to the subject an effective amount of the above-described heteromultimer or composition.

[0017] The present disclosure also provides nucleic acid sequences encoding the above heteromultimers.

[0018] There is also provided the use of the above heteromultimer in the manufacture of a medicament for the treatment of a DLL3-expressing cancer. [Brief description of the drawings]

[0019] [Figure 1] Schematic diagram of DLL3-binding heteromultimers in the following formats: B1mAb(2+1) (Figure 1A), AmAb(1+1) (Figure 1B), N1mAb(2+1) (Figure 1C), and hetero-IgG(1+1) (Figure 1D). [Figure 2A]2A-2C are graphs showing the pharmacokinetics (PK) of DLL3-binding heteromultimers ("DLL3_2") in various formats. The hetero-IgG formats ("het IgG") exhibited mAb-like PK profiles in FcRn transgenic mice following intravenous (IV) dosing at 1 mg / kg (FIG. 2A; dashed line and squares, B1 mAb; dashed line and circle, N1 mAb; dashed line and star, het IgG) and subcutaneous (SC) dosing at 1 mg / kg (FIG. 2B; dashed line and star, het IgG; dashed line and diamond, B1 mAb; solid line and triangle, N1 mAb). [Figure 2B] 2A-2C are graphs showing the pharmacokinetics (PK) of DLL3-binding heteromultimers ("DLL3_2") in various formats. The hetero-IgG formats ("het IgG") exhibited mAb-like PK profiles in FcRn transgenic mice following intravenous (IV) dosing at 1 mg / kg (FIG. 2A; dashed line and squares, B1 mAb; dashed line and circle, N1 mAb; dashed line and star, het IgG) and subcutaneous (SC) dosing at 1 mg / kg (FIG. 2B; dashed line and star, het IgG; dashed line and diamond, B1 mAb; solid line and triangle, N1 mAb). [Diagram 3] 1 is a graph showing the pharmacokinetics (PK) of DLL3-binding heteromultimer ("DLL3_1") in various formats (solid line and circle, AmAb; solid line and diamond, B1 mAb; dashed line and diamond, N1 mAb; solid line and square, N1 mAb; dashed line and cross, het IgG; dashed line and star, B1 mAb) in FcRn transgenic mice. The hetero-IgG format ("het IgG") showed a more favorable PK profile in FcRn transgenic mice after intravenous (IV) administration. [Figure 4] 4A-4B are graphs showing mean serum concentrations in female cynomolgus monkeys following administration of the DLL3-binding hetero-IgG molecule DLL3_2 either subcutaneously (FIG. 4A) or intravenously (FIG. 4B) using three different assays described in Example 4. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0020] The present disclosure is based, at least in part, on the development of multimeric proteins that target and kill DLL3-expressing tumor cells (e.g., SCLC cells, neuroendocrine prostate cancer cells, or other neuroendocrine cancer cells). The multimeric proteins further comprise a binding domain that engages and activates T cells, resulting in tumor-specific cytotoxicity. Thus, the multimeric proteins described herein may also be referred to as "multi-chain T cell engagers (mcTCEs)."

[0021] In some embodiments, the present disclosure provides a heteromultimer comprising a first heterodimer that binds to human DLL3 and a second heterodimer that binds to human CD3. For example, the first heterodimer may comprise a heavy chain (HC) comprising the amino acid sequence of SEQ ID NO:54 or SEQ ID NO:58; and a light chain (LC) comprising the amino acid sequence of SEQ ID NO:55 or SEQ ID NO:59; the second heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO:56 or SEQ ID NO:132; and a light chain comprising the amino acid sequence of SEQ ID NO:57. Without being limited by theory, it is believed that the heteromultimers described herein exhibit advantageous manufacturing properties. Such advantageous properties include, for example, high expression levels, production yields, and stability, as well as a reduction in undesired mismatched species.

[0022] definition To facilitate the understanding of the present technology, several terms and phrases are defined below. Additional definitions are set forth throughout the detailed description.

[0023] As used herein, a "multimeric protein" refers to a protein that contains two or more separate polypeptides or protein chains that associate with each other to form a single protein in vitro or in vivo. A multimeric protein may contain two or more polypeptides of the same type forming a "homomultimer". Alternatively, a multimeric protein may also be composed of two or more polypeptides of different sequences forming a "heteromultimer". Thus, a "heteromultimer" is a molecule that contains at least a first polypeptide and a second polypeptide, where the second polypeptide differs in amino acid sequence from the first polypeptide by at least one amino acid residue. A heteromultimer may include a "heterodimer" formed by a first and a second polypeptide, or may form a higher order tertiary structure in which there are three or more polypeptides.

[0024] As used herein, the term "antigen-binding protein" refers to a proteinaceous molecule that specifically binds to an antigen. For example, an antigen-binding protein may comprise an antibody or an antigen-binding fragment thereof. An antigen-binding protein typically comprises a domain that comprises or is derived from the heavy chain variable region (VH) and / or the light chain variable region (VL) of an antibody. In some embodiments, an antigen-binding protein comprises the minimum structural requirements of an antibody that allow immunospecific target binding. This minimum requirement can be defined, for example, by the presence of at least three light chain complementarity determining regions (CDRs) (i.e., CDR1, CDR2 and CDR3 of the VL region) and / or three heavy chain CDRs (i.e., CDR1, CDR2 and CDR3 of the VH region), ideally all six CDRs. Where (and in what order) those CDRs are located within the knowledge of the skilled artisan.

[0025] As used herein, the term "antibody" refers to an immunoglobulin of any isotype that has specific binding to a target antigen; the antibody may be a polyclonal or monoclonal antibody, a chimeric antibody, a humanized antibody, a human antibody, etc. In a natural antibody, the heavy chain comprises a variable region, VH, and three constant regions, CH1, CH2, and CH3. The VH domain is at the amino terminus of the heavy chain, and the CH3 domain is at the carboxy terminus. In a natural antibody, the light chain comprises a variable region, VL, and a constant region, CL. The variable region of the light chain is at the amino terminus of the light chain. In a natural antibody, the variable region of each light / heavy chain pair typically forms an antigen-binding site. The constant region is typically involved in effector functions. A natural antibody generally comprises a tetramer of two full-length heavy chains and two full-length light chains.

[0026] In human antibodies, CH1 refers to the region having the amino acid sequence at positions 118-215 of the EU index or EU numbering system, based on the consecutive numbering of the first human IgG1 (i.e., "EU antibody") to be sequenced (Edelman et al., Proc Natl Acad Sci USA, 63(1):78-85 (1969)). A highly flexible amino acid region called the "hinge region" is located between CH1 and CH2. CH2 represents the region having the amino acid sequence at positions 231-340 of the EU index, and CH3 represents the region having the amino acid sequence at positions 341-446 of the EU index.

[0027] "CL" represents the constant region of the light chain. In the case of the κ chain of a human antibody, CL represents the region having the amino acid sequence at positions 108 to 214 of the EU index. In the case of the λ chain, CL represents the region having the amino acid sequence at positions 108 to 215 of the EU index.

[0028] In natural antibodies, the variable regions typically exhibit the same general structure, with relatively conserved framework regions (FR) linked by three hypervariable regions, also called complementarity determining regions (CDRs). The CDRs from the two chains of each pair are typically aligned by framework regions that may allow binding to a specific epitope. From the N-terminus to the C-terminus, both light and heavy chain variable regions typically comprise the domains FR1, CDR1, FR2, CDR2, FR3, CDR3 and FR4. The CDRs in the heavy chain are called H1, H2 and H3, while the CDRs in the light chain are called L1, L2 and L3. Typically, CDR3 is the greatest source of molecular diversity within the antigen-binding site. The assignment of amino acids to each domain typically follows the definitions of Kabat et al. (1991) Sequences of Proteins of Immunological Interest (National Institutes of Health, Publication No. 91-3242, vols. 1-3, Bethesda, Md.); or Chothia, C., and Lesk, AM (1987) J. Mol. Biol., 196:901-917. In some embodiments, the CDRs of an antigen binding protein are defined according to the definitions of Kabat or Chothia. In this application, the term "CDR" refers to the CDRs from either the light chain or the heavy chain, unless otherwise specified.

[0029] The antibody may comprise any constant region known in the art. Human light chains are classified as kappa and lambda light chains. Heavy chains are classified as mu, delta, gamma, alpha, or epsilon, and the antibody isotypes are defined as IgM, IgD, IgG, IgA, and IgE, respectively. IgG has several subclasses, including, but not limited to, IgG1, IgG2, IgG3, and IgG4. IgM has subclasses, including, but not limited to, IgM1 and IgM2. The embodiments of the present disclosure include all such classes or isotypes of antibodies. The light chain constant region may be, for example, a kappa- or lambda-type light chain constant region, such as a human kappa- or lambda-type light chain constant region. The heavy chain constant region may be, for example, an alpha-, delta-, epsilon-, gamma-, or mu-type heavy chain constant region, such as a human alpha-, human delta-, human epsilon-, human gamma-, or human mu-type heavy chain constant region. Thus, in exemplary embodiments, the antibody is of the isotype IgA, IgD, IgE, IgG or IgM, including any one of IgG1, IgG2, IgG3 or IgG4.

[0030] The antibody may be a monoclonal or polyclonal antibody. As used herein, the term "monoclonal antibody" refers to an antibody produced by a single clone of B lymphocytes directed against a single epitope on an antigen. Monoclonal antibodies are typically produced using hybridoma technology as first described in Kohler and Milstein, Eur. J. Immunol., 5:511-519 (1976). Monoclonal antibodies can also be produced using recombinant DNA methods (see, e.g., U.S. Pat. No. 4,816,567), isolated from phage display antibody libraries (see, e.g., Clackson et al. Nature, 352:624-628 (1991); and Marks et al., J. Mol. Biol., 222:581-597 (1991)), or produced from transgenic mice with a fully human immunoglobulin system (see, e.g., XENOMOUSE™ mice, Green et al. (1994) Nature Genetics 7:13-21, U.S. Patent Publication No. 2003-0070185, WO 96 / 34096, and WO 96 / 33735). In contrast, "polyclonal" antibodies are antibodies secreted by different B cell lineages within an animal. Polyclonal antibodies are a population of immunoglobulin molecules that recognize multiple epitopes on the same antigen.

[0031] The term "chimeric antibody" refers to an antibody that contains domains from two or more different antibodies. A chimeric antibody may, for example, contain a constant domain from one species and a variable domain from a second species, or more commonly, a stretch of amino acid sequence from at least two species. A chimeric antibody may also contain domains from two or more different antibodies within the same species. The term "humanized" when used in reference to an antibody refers to an antibody with at least the CDR regions from a non-human source that have been modified to have a structure and immune function more similar to a true human antibody than the original source antibody. For example, humanization may involve grafting CDRs from a non-human antibody, such as a mouse antibody, onto a human antibody. Humanization may also involve selecting amino acid substitutions to make the non-human sequence more similar to the human sequence.

[0032] Antibodies can be cleaved into fragments by enzymes such as, for example, papain and pepsin. Papain cleaves antibodies to produce two Fab fragments and an Fc fragment. Pepsin cleaves antibodies to generate a F(ab')2 fragment and a pFc' fragment. In an exemplary embodiment, the antigen-binding proteins of the present disclosure comprise an antigen-binding antibody fragment. As used herein, the term "antigen-binding antibody fragment" refers to a portion of an antibody molecule capable of binding to the antigen of the antibody, also known as an "antigen-binding fragment" or "antigen-binding portion." In an exemplary example, the antigen-binding antibody fragment is a Fab fragment or a F(ab')2 fragment.

[0033] The structure of antibodies spans a molecular weight range of at least about 12-150 kDa and has been exploited to create a growing range of alternative formats ranging from monomers (n=1) to dimers (n=2), trimers (n=3), tetramers (n=4) and potentially higher valencies (n), which are referred to herein as "antibody protein products." Antibody protein products include those based on the complete antibody structure and those that mimic antibody fragments that retain full antigen-binding ability, such as scFv, Fab and VHH / VH (discussed below). The smallest antigen-binding antibody fragment that retains an intact antigen-binding site is an Fv fragment consisting entirely of the variable (V) region. Soluble, flexible amino acid peptide linkers are used to link the V region to scFv (single chain fragment variable) fragments to stabilize the molecule, or constant (C) domains are added to the V region to generate Fab fragments. Both scFv and Fab fragments can be readily produced in host cells (e.g., prokaryotic host cells). Other antibody protein products include dimeric and multimeric antibody formats such as diabodies, triabodies, and tetrabodies, or minibodies (miniAbs), including disulfide bond stabilized scFv (ds-scFv), single chain Fab (scFab), and different formats consisting of scFv linked to oligomerization domains. Peptibodies or peptide-Fc fusions are yet another antibody protein product. The structure of a peptibody consists of a biologically active peptide grafted to an Fc domain. Peptibodies are well described in the art (see, for example, Shimamoto et al., mAbs 4(5):586-591(2012)).

[0034] The antigen-binding heteromultimer of the present disclosure may comprise any one of the antibody protein products described above. In an exemplary embodiment, the antigen-binding heteromultimer of the present disclosure comprises any one of scFv, Fab, VHH / VH, Fv fragment, ds-scFv, scFab, dimeric antibody, multimeric antibody (e.g., diabody, triabody, tetrabody), miniAb, camelid heavy chain antibody peptibody VHH / VH, sdAb, diabody; triabody; tetrabody; bispecific or trispecific antibody, BsIgG, appended IgG, BsAb fragment, bispecific fusion protein, and BsAb conjugate.

[0035] In certain embodiments, the multimeric antigen-binding proteins of the present disclosure may be "bispecific," meaning that they can specifically bind to two different antigens. In another embodiment, the multimeric antigen-binding proteins of the present disclosure may be "trispecific," meaning that they can specifically bind to three different antigens. In another embodiment, the multimeric antigen-binding proteins of the present disclosure may be "tetraspecific," meaning that they can specifically bind to four different antigens. As used herein, an antigen-binding protein "specifically binds" to a target antigen if it has a significantly higher binding affinity for the target antigen compared to its affinity for other unrelated proteins under similar binding assay conditions, such that it can discriminate between the antigens. An antigen-binding protein that specifically binds to an antigen has a binding affinity of ≦1×10 -6 The equilibrium dissociation constant of M (K D In an exemplary embodiment, the K of the antigen binding proteins provided herein may be D is micromolar, nanomolar, picomolar or femtomolar. The antigen-binding protein has a K D is ≦3×10 -8 In some embodiments, the antigen-binding protein of the disclosure specifically binds to an antigen with "high affinity" when M is ≤ 100 nm (e.g., 90 nm, 80 nm, 70 nm, 60 nm, 50 nm, 40 nm, 30 nm, 20 nm, 10 nm, 5 nm, or a range defined by any two of the above values). DIn other embodiments, the antigen binding proteins of the disclosure bind to a target antigen with a K of about 10 nm to 30 nm (e.g., about 15 nm, 20 nm, or 25 nm). D and binds to the target antigen.

[0036] Affinity can be determined by a variety of techniques, one example of which is enzyme-linked immunosorbent assay (ELISA). In various embodiments, affinity is determined by a surface plasmon resonance assay (e.g., a BIACORE®-based assay). Using this methodology, the binding rate constant (k a Unit:M -1 s -1 ) and dissociation rate constant (k d Unit: s -1 ) can then be measured. D The ratio of kinetic rate constants (k d / k a ) can be calculated from the equilibrium dissociation constant (K ). In some embodiments, affinity can be determined by kinetic methods, such as Kinetic Exclusion Assay (KinExA), as described in Rathanaswami et al., Analytical Biochemistry, 373:52-60 (2008). The KinExA assay can be used to determine the equilibrium dissociation constant (K D Unit: M) and association rate constant (ka unit: M -1 s -1 The dissociation rate constant (k d Unit: s -1 ) are these values ​​(K D ×k a ) to a target antigen expressed by mammalian cells (e.g., CHO, HEK293, Jurkat), as determined by the equilibrium exclusion method (Rathanaswami et al., supra).-8 M) K below D , 10 nM (1.0 × 10 -8 M) K below D , 1 nM (1.0 × 10 -9 M) K below D , 500pM (5.0×10 -10 M) K below D , 200pM (2.0×10 -10 M) K below D , 150 pM (1.50 × 10 -10 M) K below D , 125 pM (1.25 × 10 -10 M) K below D , 105 pM (1.05 × 10 -10 M) K below D , 50 pM (5.0 × 10 -11 M) K below D , or 20 pM (2.0 × 10 -11 M) K below D In some embodiments, the multimeric antigen binding proteins described herein specifically bind at k d The binding avidity for the target antigen, as measured by -2 , 10 -3 , 10 -4 , 10 -5 , 10 -6 , 10 -7 , 10 -8 , 10 -9 , 10 -10 s -1 or less (lower values ​​indicate higher binding avidity), and / or K D The binding affinity for the target antigen, as measured by -9 , 10 -10 , 10 -11 , 10 -12 , 10 -13 , 10 -14 , 10 -15 , 10 -16 M or less (lower values ​​indicate higher binding affinity).

[0037] In certain embodiments of the present disclosure, the antigen binding protein may be multivalent. The valency of a binding protein indicates the number of individual antigen binding domains within the binding protein. In some embodiments, a bispecific antigen binding protein may be multivalent. For example, in certain embodiments, a bispecific antigen binding protein may be tetravalent by comprising four antigen binding domains: two antigen binding domains that bind to a first target antigen and two antigen binding domains that bind to a second target antigen. A tetraspecific antigen binding protein is tetravalent and comprises four antigen binding domains: one antigen binding domain that binds to a first target antigen, one antigen binding domain that binds to a second target antigen, one antigen binding domain that binds to a third target antigen, and one antigen binding domain that binds to a fourth target antigen.

[0038] As used herein, the term "antigen binding domain", used synonymously with "binding domain", refers to a region of an antigen binding protein that contains amino acid residues that interact with an antigen and confer specificity and affinity to the antigen binding protein for that antigen. In some embodiments, the binding domain may be derived from a natural ligand of the target antigen. As used herein, the term "target antigen" refers to the first and / or second target antigen of a bispecific molecule, and also to the first, second, third and / or fourth target antigen of a tetraspecific molecule.

[0039] As used herein, the term "immunoglobulin domain" refers to a peptide that contains an amino acid sequence similar to that of an immunoglobulin and contains about 100 amino acid residues including at least two cysteine ​​residues. Examples of immunoglobulin domains include, for example, VH, CH1, CH2 and CH3 of an immunoglobulin heavy chain, and VL and CL of an immunoglobulin light chain. In addition, immunoglobulin domains are found in proteins other than immunoglobulins. Examples of immunoglobulin domains in proteins other than immunoglobulins include immunoglobulin domains contained in proteins belonging to the immunoglobulin superfamily, such as major histocompatibility complex (MHC), CD1, B7, T cell receptor (TCR), etc. Any of the immunoglobulin domains can be used as the immunoglobulin domain of the multimeric proteins described herein.

[0040] The binding domains that specifically bind to the target antigens can be derived from a) known antibodies against these antigens, or b) new antibodies or antibody fragments obtained by novel immunization methods using antigenic proteins or fragments thereof, by phage display, or by other conventional methods. The antibody from which the binding domains of the antigen-binding proteins originate can be a monoclonal antibody, a polyclonal antibody, a recombinant antibody, a human antibody, or a humanized antibody. In certain embodiments, the antibody from which the binding domains originate is a monoclonal antibody. In these and other embodiments, the antibody is a human antibody or a humanized antibody and can be of the IgG1, IgG2, IgG3, or IgG4 type.

[0041] As used herein, the terms "stability" and "stabilization" are defined as the maintenance of the chemical or physical integrity and / or biological activity of an antigen-binding polypeptide or protein over a period of time. Stabilization of an antigen-binding polypeptide or protein includes preventing or slowing the decomposition or degradation of an antigen-binding polypeptide or protein from its biologically and / or therapeutically active form to an inactive form. Instability can result from events such as aggregation, denaturation, fragmentation, or chemical modifications, such as oxidation, cross-linking, deamidation, and reaction with other components present in a composition comprising the antigen-binding polypeptide or protein.

[0042] The stability of an antigen binding protein or polypeptide can be characterized using methods known in the art, including, but not limited to, measuring biological activity such as antigen binding activity by immunoassay techniques such as ELISA, or other techniques that determine purity or physical / chemical changes to the antigen binding protein or polypeptide, such as size exclusion chromatography, capillary gel electrophoresis, circular dichroism or mass spectrometry. Stability is determined by comparison of measurements obtained by these types of characterization methods at an earlier time point, such as upon formulation or preparation of the composition (i.e., suspension or dispersion, as the case may be), to measurements obtained at a later time point, i.e., after storage in a given environment or condition.

[0043] As used herein, the term "CD3 receptor complex" refers to a protein complex composed of four chains. In mammals, this complex contains the CD3γ (gamma) chain, the CD3δ (delta) chain, and two CD3ε (epsilon) chains. These chains associate with the T cell receptor (TCR) and the so-called ζ (zeta) chain to form the T cell receptor-CD3 complex, which generates an activation signal in T lymphocytes. The CD3γ (gamma), CD3δ (delta), and CD3ε (epsilon) chains are very closely related cell surface proteins of the immunoglobulin superfamily that contain a single extracellular immunoglobulin domain. The intracellular tail of the CD3 molecule contains a single conserved motif known as the immunoreceptor tyrosine-based activation motif or ITAM for short, which is essential for the signaling ability of the TCR. The CD3 epsilon molecule is a polypeptide encoded by the CD3E gene, which in humans is present on chromosome 11. The most preferred epitope of CD3 epsilon is contained within amino acid residues 1 to 27 of the extracellular domain of human CD3 epsilon.

[0044] Drugs that target DLL3 Delta-like ligand 3 (DLL3) is a non-canonical Notch ligand expressed primarily during embryonic development that functions during somitogenesis. DLL3 accumulates in the Golgi apparatus in normal tissues (Geffers et al, J Cell Biol. 178:465-476 (2007)). DLL3 was identified as a tumor-associated antigen and a target for T cell-based therapy by analyzing its differential expression in SCLC tumors and a wide range of normal tissues (Saunders et al., supra; Giffin et al., J Thorac Oncol., 13(10):S971 (2018)). Human DLL3 protein contains several extracellular domains: signal peptide, N-terminus, DSL, EGF1, EGF2, EGF3, EGF4, EGF5, EGF6, and membrane proximal domain. Exemplary amino acid sequences of human DLL3 include, for example, UniProt Q9NYJ7 and NCBI reference sequence: NP_058637.1.

[0045] One example of an agent that targets DLL3 is a bispecific T cell-inducing antigen-binding polypeptide that binds DLL3 and CD3, such as a BiTE® molecule. A BiTE® molecule is a recombinant protein that contains two flexibly linked binding domains, each derived from an antibody. One binding domain of the BiTE® molecule is specific for a tumor-associated surface antigen (e.g., DLL3), and the second binding domain is specific for CD3, a subunit of the T cell receptor complex on T cells. These designs make the BiTE® molecule uniquely suitable for transiently binding T cells to target cells while simultaneously potently activating the innate cytotoxicity of T cells against target cells. See, for example, WO 99 / 54440, WO 2005 / 040220, and WO 2008 / 119567.

[0046] AMG 757 (Tallatamab) is a half-life extended (HLE) BiTE® molecule developed for the treatment of SCLC. The activity of AMG 757 requires simultaneous binding to both target cells (DLL3+ cells) and T cells. The pharmacological effect of AMG 757 is mediated by the specific redirection of already primed cytotoxic CD8+ or CD4+ T lymphocytes to kill DLL3+ cells. AMG 757 has shown antitumor activity in patients with SCLC in Phase 1 trials and is currently undergoing clinical evaluation (see, e.g., ClinicalTrials.gov. Identification Number: NCT03319940 and Pax-Ares et al., J Clin Oncol, JCO2202823. doi:10.1200 / JCO.22.02823(2023)).

[0047] In some embodiments, the heteromultimers provided herein are heterodimeric antibodies (used interchangeably herein as "heteroimmunoglobulins" or "heteroIgs"), which are antibodies that comprise two different light chains and two different heavy chains. Exemplary heteromultimers encompassed by the present disclosure include a first heterodimer that binds to human DLL3 and a second heterodimer that binds to human CD3. In some embodiments, the first heterodimer comprises a heavy chain (HC) comprising the amino acid sequence of SEQ ID NO:54 or SEQ ID NO:58 and a light chain (LC) comprising the amino acid sequence of SEQ ID NO:55 or SEQ ID NO:59; the second heterodimer comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:56 or SEQ ID NO:132; and a light chain comprising the amino acid sequence of SEQ ID NO:57. For example, the first heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO:54 and a light chain comprising the amino acid sequence of SEQ ID NO:55. Alternatively, the first heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO:58 and a light chain comprising the amino acid sequence of SEQ ID NO:59. In some embodiments, for example, the second heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO: 56 and a light chain comprising the amino acid sequence of SEQ ID NO: 57. In other embodiments, for example, the second heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO: 132 and a light chain comprising the amino acid sequence of SEQ ID NO: 57. In some embodiments, the first heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO: 60. In further embodiments, the second heterodimer may comprise a heavy chain comprising the amino acid sequence of SEQ ID NO: 133.

[0048] Thus, exemplary heteromultimers provided herein can include a first heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO: 54 and a light chain amino acid sequence of SEQ ID NO: 55; and a second heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO: 56 and a light chain amino acid sequence of SEQ ID NO: 57. In other embodiments, exemplary heteromultimers provided herein can include a first heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO: 54 and a light chain amino acid sequence of SEQ ID NO: 55; and a second heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO: 132 and a light chain amino acid sequence of SEQ ID NO: 57. In some embodiments, exemplary heteromultimers provided herein include a first heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO: 58 and a light chain amino acid sequence of SEQ ID NO: 59; and a second heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO: 56 and a light chain amino acid sequence of SEQ ID NO: 57. In other embodiments, exemplary heteromultimers provided herein include a first heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO:58 and a light chain amino acid sequence of SEQ ID NO:59; and a second heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO:132 and a light chain amino acid sequence of SEQ ID NO:57.

[0049] In some embodiments, the heteromultimer binds to the EGFR5 and EGFR6 extracellular domains of the human DLL3 protein.

[0050] In some embodiments, the disclosed heteromultimers may comprise a first heterodimer comprising a heavy chain amino acid sequence that is at least 90% identical (e.g., at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO:54 or SEQ ID NO:58, and / or a light chain amino acid sequence that is at least 90% identical (e.g., at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO:55 or SEQ ID NO:59. In other embodiments, the disclosed heteromultimers may comprise a second heterodimer comprising a heavy chain amino acid sequence that is at least 90% identical (e.g., at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO:56 or SEQ ID NO:132, and / or a light chain amino acid sequence that is 90% identical (e.g., at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% identical) to SEQ ID NO:57.

[0051] Nucleic acid or amino acid sequence "identity" can be determined by comparing a subject nucleic acid or amino acid sequence to a reference nucleic acid or amino acid sequence. The percent identity is the number of nucleotides or amino acid residues that are the same (i.e., identical) between the subject and reference sequences, divided by the length of the longest sequence (i.e., the length of either the subject sequence or the reference sequence, whichever is longer). Several mathematical algorithms for obtaining optimal alignment and calculating the identity between two or more sequences are known and are incorporated into several available software programs. Examples of such programs include CLUSTAL Omega, T-Coffee, and ALIGN (for alignment of nucleic acid and amino acid sequences), BLAST programs (e.g., BLAST 2.13, BL2SEQ, and their more recent versions), and FASTA programs (e.g., FASTA3x, FASTM, and S SEARCH) (for sequence alignment and sequence similarity search). Sequence alignment algorithms are also described in, e.g., Altschul et al., J. Molecular Biol, 275(3):403-410 (1990); Beigert et al., Proc. Natl. Acad. Sci. USA, 106(10):3770-3775 (2009); Durbin et al., eds., Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids, Cambridge University Press, Cambridge, UK (2009); Soding, Bioinformatics, 27(7):951-960 (2005); Altschul et al., Nucleic Acids Res., 25(17):3389-3402 (1997); and Gusfield, Algorithms on Strings, Trees and Sequences, Cambridge University Press, Cambridge This was disclosed in the UK (1997).

[0052] The heteromultimers described herein may include any immunoglobulin constant region. As used herein, the term "constant region" refers to all domains other than the variable region of an antibody. The constant region is not directly involved in antigen binding, but exerts various effector functions. As explained above, antibodies are divided into specific isotypes (IgA, IgD, IgE, IgG, and IgM) and subtypes (IgG1, IgG2, IgG3, IgG4, IgA1, IgA2) depending on the amino acid sequence of the constant region of their heavy chain. The light chain constant region may be, for example, a kappa or lambda light chain constant region, e.g., a human kappa or lambda light chain constant region, which are found in all five isotypes of antibodies. In some embodiments, the heteromultimers disclosed herein are of the IgG1 or IgG4 isotype.

[0053] The natural formation of the Fc region of an IgG molecule involves the assembly of two matching Fc chains, independent of the sequence of the antigen-binding (Fab) arms. As explained above, bispecific antibodies have target specificity for two or more different antigens. This is due to the two Fab arms having different sequences. As a result, bispecific molecules with natural Fc regions tend to assemble into three main types of heavy chain molecules: monoclonal antibodies that bind one antigen, monoclonal antibodies that bind a second antigen, and bispecific antibodies that bind both antigens.

[0054] In some embodiments, two different heavy chains are used to form the first and second heterodimers of the present disclosure. To facilitate assembly of the light and heavy chains into a heterodimeric antibody, the light and / or heavy chains from each antibody can be engineered to reduce the formation of mismatched molecules. For example, one approach to promote heterodimer formation over homodimer formation is the so-called "knobs-into-holes" method, which involves introducing mutations into the CH3 domains of two different antibody heavy chains at the contact interface. Specifically, one or more bulky amino acids in one heavy chain are replaced with amino acids with short side chains (e.g., alanine or threonine) to generate a "hole," while one or more amino acids with large side chains (e.g., tyrosine or tryptophan) are introduced into the other heavy chain to generate a "knob." When the modified heavy chains are co-expressed, a higher percentage of heterodimers (knobs-holes) are formed compared to homodimers (hole-hole or knob-knobs). The "knobs-into-holes" methodology is described in detail in WO 96 / 027011; Ridgway et al., Protein Eng., Vol. 9:617-621, 1996; and Merchant et al., Nat. Biotechnol., Vol. 16:677-681, 1998.

[0055] Another approach to promote heterodimer formation and eliminate homodimer formation involves utilizing an electrostatic steering mechanism (Gunasekaran et al., J. Biol. Chem., Vol. 285:19637-19646, 2010). This approach involves introducing or utilizing charged residues in the CH3 domains in each heavy chain so that two different heavy chains associate due to opposite charges that cause electrostatic attraction. Homodimerization of identical heavy chains is unfavorable because identical heavy chains have the same charge and are therefore repelled. This same electrostatic steering technique can be used to prevent mispairing of light chains with non-cognate heavy chains by introducing oppositely charged residues into the binding interface for appropriate light-heavy chain pairs. Electrostatic steering techniques and suitable charge pair mutations (CPM) to promote heterodimerization and proper light chain / heavy chain pairing are described, for example, in WO 2009 / 089004, WO 2014 / 081955, and WO 2021 / 092355.

[0056] In embodiments where a heteromultimeric antigen binding protein of the disclosure comprises a first light chain (LC1) and a first heavy chain (HC1) from a first antibody that specifically binds to a first target antigen, and a second light chain (LC2) and a second heavy chain (HC2) from a second antibody that specifically binds to target 2, HC1 or HC2 may comprise one or more amino acid substitutions that replace a positively charged amino acid with a negatively charged amino acid. For example, in one embodiment, the CH3 domain of HC1 or the CH3 domain of HC2 comprises an amino acid sequence that differs from the wild-type human IgG amino acid sequence such that one or more positively charged amino acids (e.g., lysine, histidine, and arginine) in the wild-type IgG amino acid sequence are replaced with one or more negatively charged amino acids (e.g., aspartic acid and glutamic acid) at the corresponding positions in the CH3 domain.

[0057] In exemplary embodiments, the heavy chain constant region of the first heterodimer disclosed herein may comprise amino acid substitutions at positions 183, 392, 409, and / or 439, and the second heterodimer may comprise amino acid substitutions at positions 183, 356, and / or 399, as numbered according to the EU index. In some embodiments, the heavy chain constant region of the first heterodimer comprises amino acid substitutions S183K, K392D, K409D, and K439D, and the heavy chain constant region of the second heterodimer comprises amino acid substitutions S183E, E356K, and D399K. In other embodiments, the light chain constant regions of the first and second heterodimers comprise an amino acid substitution at position 176, such as, for example, S176K. It will be appreciated that other amino acid modifications may be made to the heteromultimers described herein to extend half-life, improve stability and / or developability. Such modifications include, but are not limited to, YTE and / or SEFL2 modifications (Dall'Acqua et al., The Journal of Immunology, 169:5171-5180 (2002); Jacobsen et al., The Journal of Biological Chemistry, 292(3):1865-1875 (2017)). As explained above, the heteromultimers described herein exhibit advantageous manufacturing properties including, for example, high expression levels and production yields, increased stability, and reduced undesired mismatched species.

[0058] Compositions and kits The present disclosure provides a composition comprising a heteromultimer as described herein and a carrier therefor (e.g., a pharma- ceutically acceptable carrier). The composition is desirably a physiologically acceptable (e.g., pharma- ceutical) composition comprising a carrier, preferably a physiologically (e.g., pharma- ceutical) acceptable carrier, and a heteromultimer. Any suitable carrier may be used within the context of the present disclosure, and such carriers are well known in the art. The choice of carrier will be determined, in part, by the particular use of the composition (e.g., administration to a human) and the particular method used to administer the composition.

[0059] As used herein, the term "pharmaceutical acceptable carrier" includes any of the standard pharmaceutical carriers, such as phosphate buffered saline, water, emulsions such as oil / water or water / oil emulsions, and various types of wetting agents. The term also encompasses any of the agents approved by a regulatory agency of the U.S. Federal government or listed in the United States Pharmacopeia for use in animals, including humans.

[0060] The pharmaceutical composition may contain, for example, an acidifying agent, an additive, an adsorbent, an aerosol propellant, an exhaust agent, an alkalizing agent, an anti-caking agent, an anticoagulant, an antimicrobial preservative, an antioxidant, a preservative, a base, a binder, a buffer, a chelating agent, a coating agent, a coloring agent, a drying agent, a surfactant, a diluent, a disinfectant, a disintegrant, a dispersant, a dissolution enhancer, a dye, a softener, an emulsifier, an emulsion stabilizer, a filler, a film former, a flavor enhancer, a flavoring, a glidant, a gelling agent, a forming agent, a stimulant ... Any pharma- ceutically acceptable ingredient may be included, including granules, humectants, lubricants, mucoadhesives, ointment bases, ointments, oily vehicles, organic bases, pastille bases, pigments, plasticizers, abrasives, preservatives, sequestering agents, skin-penetrating agents, solubilizers, solvents, stabilizers, suppository bases, surface active agents, surfactants, suspending agents, sweeteners, therapeutic agents, thickening agents, isotonicity agents, toxicity agents, viscosity-increasing agents, water-absorbing agents, water-miscible cosolvents, water-softening agents, or humectants. See, for example, the Handbook of Pharmaceutical Excipients, Third Edition, A.H. Kibbe (Pharmaceutical Press, London, UK, 2000); and Remington's Pharmaceutical Sciences, Sixteenth Edition, E.W. Martin (Mack Publishing Co., Easton, Pa., (1980)).

[0061] In exemplary embodiments, the composition may include components that are non-toxic to recipients at the dosages and concentrations utilized. For example, the composition may include an active agent and one or more pharma- ceutically acceptable salts, polyols, surfactants, osmotic balancing agents, isotonicity agents, antioxidants, antibiotics, antifungal agents, bulking agents, lyoprotectants, antifoaming agents, chelating agents, preservatives, coloring agents, analgesics, or additional medicinal agents. In exemplary embodiments, the composition may optionally include one or more excipients, such as, but not limited to, pharma- ceutically acceptable salts; osmotic balancing agents (isotonicity agents); antioxidants; antibiotics; antifungal agents; bulking agents; lyoprotectants; antifoaming agents; chelating agents; preservatives; coloring agents; and analgesics, in addition to one or more polyols and / or one or more surfactants.

[0062] In certain embodiments, the compositions can contain formulation materials to alter, maintain or preserve, for example, the pH, osmolality, viscosity, clarity, color, isotonicity, odor, sterility, stability, dissolution or release rate, adsorption, or permeability of the composition. In such embodiments, suitable formulation materials include amino acids (such as glycine, glutamine, asparagine, arginine, or lysine); antimicrobial agents; antioxidants (such as ascorbic acid, sodium sulfite, or sodium bisulfite); buffers (such as boric acid, bicarbonate, Tris-HCl, citric acid, phosphoric acid, or other organic acids); bulking agents (such as mannitol or glycine); chelating agents (such as ethylenediaminetetraacetic acid (EDTA)); complexing agents (such as caffeine, polyvinylpyrrolidone, beta-cyclodextrin, or hydroxypropyl-beta-cyclodextrin); fillers; monosaccharides; disaccharides; and other carbohydrates (such as glucose, mannose, or dextrin); proteins (such as serum albumin, gelatin, or immunoglobulins); colorants, flavoring agents, and diluents; emulsifiers; hydrophilic polymers (such as polyvinylpyrrolidone); low molecular weight polypeptides; salt-forming counterions (such as sodium preservatives (such as benzalkonium chloride, benzoic acid, salicylic acid, thimerosal, phenethyl alcohol, methylparaben, propylparaben, chlorhexidine, sorbic acid or hydrogen peroxide); solvents (such as glycerin, propylene glycol or polyethylene glycol); sugar alcohols (such as mannitol or sorbitol); suspending agents; surfactants or wetting agents (pluronic®, PEG, sorbitan esters, polysorbates such as polysorbate 20, polysorbate 80, triton, tromethamine, lecithin, cholesterol, tyloxapol); stabilization enhancers; isotonicity enhancers (such as alkali metal halides, preferably sodium or potassium chloride, mannitol sorbitol); delivery vehicles; diluents; excipients and / or pharmaceutical adjuvants (e.g., Remington's See Pharmaceutical Sciences, Sixteenth Edition, E. W. Martin, Mack Publishing Co., Easton, Pa., (1980).

[0063] The compositions may be formulated to achieve a physiologically compatible pH, in some embodiments, for example, the pH of the composition may be about 4 to about 8 (e.g., about 4.5, 5.0, 5.5, 6.0, 6.5, 7.0, 7.5, or a range defined by any two of the above values).

[0064] In some embodiments, the composition is formulated based on the intended delivery route. For example, in certain embodiments, the pharmaceutical composition is formulated for parenteral delivery. Parenteral delivery forms include intravenous, intraarterial, subcutaneous, intrathecal, intraperitoneal, and intramuscular injection or infusion. In some embodiments, the composition is formulated for intravenous delivery. In such embodiments, the composition may include a lipid-based delivery vehicle. In other embodiments, the composition is formulated for subcutaneous or transdermal delivery.

[0065] In some embodiments, the composition comprises an effective amount of a heteromultimer described herein, e.g., a "therapeutically effective amount." A "therapeutically effective amount" is an amount sufficient to produce a beneficial or desired clinical outcome. In some embodiments, a therapeutically effective amount is an amount sufficient to kill DLL3-expressing tumor cells in a subject. In other embodiments, a therapeutically effective amount of a heteromultimer desirably reduces the severity of disease (e.g., cancer) symptoms, increases the frequency or duration of disease symptom-free periods, or prevents impairment or disability due to disease affliction. In some embodiments, a therapeutically effective amount of a heteromultimer inhibits cancer cell growth or tumor growth by at least about 20%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, or at least about 90% compared to an untreated subject. The ability of a compound to inhibit tumor growth can be evaluated in animal models that are predictive of efficacy in human tumors.

[0066] Typical doses can range from about 1 μg up to about 500 mg or more, depending on the factors described above. For example, a daily parenteral dose can be about 2 mg or more, e.g., about 3 mg to about 500 mg, about 10 mg to about 200 mg, or about 50 mg to about 100 mg. However, it will be understood that doses less than or greater than these exemplary ranges are within the scope of the present disclosure. In some embodiments, the dose of the heteromultimer present in the composition can be about 100 mg or less (e.g., about 90 mg, about 80 mg, about 70 mg, about 60 mg, about 50 mg, about 40 mg, about 30 mg, about 20 mg, about 10 mg, or a range defined by any two of the above values). In other embodiments, the dose of the heteromultimer present in the composition can be about 10 mg or less (e.g., about 9 mg, about 5 mg, about 1 mg, about .5 mg, about 100 μg, about 1 μg, or a range defined by any two of the above values). In some embodiments, a composition comprising the heteromultimer, or the heteromultimer itself, may be administered to a subject (e.g., a human) at a dose of about 3 mg to about 100 mg (e.g., about 3 mg, about 5 mg, about 10 mg, about 15 mg, about 25 mg, about 35 mg, about 45 mg, about 55 mg, about 65 mg, about 75 mg, about 85 mg, about 95 mg, or a range defined by any two of the above values) at least once a week. For example, a composition comprising the heteromultimer, or the heteromultimer itself, may be administered to a human at least once every two weeks, at least once every three weeks, at least once every four weeks, etc.

[0067] The heteromultimer may be provided in the form of a kit, i.e., a packaged combination of a predetermined amount of reagents together with instructions for use. In an exemplary embodiment, the kit may include the heteromultimer, or a composition comprising the same, in a container. In an exemplary embodiment, the heteromultimer, or a composition comprising the same, is provided in the kit as a unit dose. As used herein, the term "unit dose" refers to a discrete amount dispersed in a suitable carrier. In an exemplary embodiment, the unit dose is an amount sufficient to provide a desired effect in a subject, such as a therapeutically effective amount as described above. In an exemplary embodiment, the kit may include several unit doses, for example, optionally a weekly or monthly supply of unit doses, each unit dose being individually packaged or otherwise separated from other unit doses. In some embodiments, the components of the kit / unit dose are packaged together with instructions for administration to a patient. In some embodiments, the kit includes one or more devices for administration to a patient, such as a needle and a syringe. In some embodiments, the heteromultimer, or a composition comprising the same, is prepackaged in a ready-to-use form, such as a syringe, an intravenous bag, and the like. In exemplary embodiments, the ready-to-use form is for single use. In exemplary embodiments, the kit includes a ready-to-use form of the disclosed heteromultimer, or a composition comprising the same, for multiple single use. In some embodiments, the kit may further include other therapeutic or diagnostic agents or pharma- ceutically acceptable carriers (e.g., solvents, buffers, diluents, etc.), including any of those described herein.

[0068] Nucleic Acids and Vectors The present disclosure also provides one or more nucleic acid sequences encoding the heteromultimers described herein. The term "nucleic acid sequence" encompasses polymers of DNA or RNA, i.e., polynucleotides, which may be single-stranded or double-stranded and may contain non-natural or modified nucleotides. As used herein, the terms "nucleic acid" and "polynucleotide" refer to polymeric forms of nucleotides of any length, either ribonucleotides (RNA) or deoxyribonucleotides (DNA). These terms refer to the primary structure of the molecule and thus include double-stranded and single-stranded DNA, as well as double-stranded and single-stranded RNA. The terms include as equivalents analogs of either RNA or DNA made from nucleotide analogs, as well as modified polynucleotides, such as, but not limited to, methylated and / or end-protected polynucleotides. Nucleic acids are typically linked via phosphate linkages to form nucleic acid sequences or polynucleotides, although many other linkages are known in the art (e.g., phosphorothioates, boranophosphates, etc.).

[0069] In some aspects, the disclosure provides one or more nucleic acid sequences encoding the heavy and light chains of a first heterodimer. For example, a first nucleic acid sequence may encode the heavy chain of the first heterodimer, and a second nucleic acid sequence different from the first nucleic acid sequence may encode the light chain of the first heterodimer. Alternatively, both the heavy and light chains of the first heterodimer may be encoded by a single nucleic acid sequence. Similarly, a first nucleic acid sequence may encode the heavy chain of the second heterodimer, and a second different nucleic acid sequence may encode the light chain of the second heterodimer. Alternatively, both the heavy and light chains of the second heterodimer may be encoded by a single nucleic acid sequence. In other aspects, a single nucleic acid sequence may encode the heavy and light chains of the first heterodimer and the heavy and light chains of the second heterodimer. Exemplary nucleic acid sequences encoding the CDRs, variable regions, and heavy and light chains that bind DLL3 and human CD3 are set forth below in Sequence Tables 15 and 15A.

[0070] The present disclosure further provides a vector comprising one or more nucleic acid sequences encoding a heteromultimer, or a component thereof (e.g., a first heterodimer and / or a second heterodimer). The vector can be, for example, a plasmid, an episome, a cosmid, a viral vector (e.g., a retrovirus or an adenovirus), or a phage. Suitable vectors and methods for vector preparation are well known in the art (see, for example, Sambrook et al., Molecular Cloning, a Laboratory Manual, 3rd edition, Cold Spring Harbor Press, Cold Spring Harbor, NY (2001), and Ausubel et al., Current Protocols in Molecular Biology, Greene Publishing Associates and John Wiley & Sons, New York, NY (1994)).

[0071] The heteromultimers described herein can be produced by recombinant DNA methods known in the art. As used herein, "recombinant" means that a particular nucleic acid (DNA or RNA) is the product of various combinations of cloning, restriction, polymerase chain reaction (PCR) and / or ligation steps that result in a construct with structural coding or non-coding sequences that are distinguishable from endogenous nucleic acids found in natural systems. DNA sequences encoding polypeptides can be assembled from cDNA fragments or from a series of synthetic oligonucleotides to generate synthetic nucleic acids that can be expressed from recombinant transcription units contained in cells or cell-free transcription and translation systems. Genomic DNA containing relevant sequences can also be used to form recombinant genes or transcription units. Sequences of non-translated DNA can be present 5' or 3' from the open reading frame, where such sequences do not interfere with the manipulation or expression of the coding region and may in fact function to regulate the production of the desired product by various mechanisms). Alternatively, DNA sequences that are not translated, encoding RNA (e.g., DNA-targeting RNA), can also be considered recombinant. Thus, the term "recombinant" nucleic acid refers to one that is not natural, e.g., one that is created by the artificial combination of two originally separated segments of sequence by human intervention. This artificial combination is often achieved by chemical synthesis means or by the artificial manipulation of isolated segments of nucleic acid, e.g., by recombinant genetic techniques. This is usually done by replacing codons with codons that code for the same amino acid, conservative amino acids, or non-conservative amino acids. Alternatively, it is done by joining together nucleic acid segments of desired functions to generate a desired combination of functions. This artificial combination is often achieved by chemical synthesis means or by the artificial manipulation of isolated segments of nucleic acid, e.g., by recombinant genetic techniques. When a recombinant polynucleotide encodes a polypeptide, the sequence of the encoded polypeptide can be natural ("wild type") or can be a variant (e.g., mutant) of the natural sequence. Thus, the term "recombinant" polypeptide does not necessarily refer to a polypeptide whose sequence does not exist in nature.Alternatively, a "recombinant" polypeptide is encoded by a recombinant DNA sequence, but the sequence of the polypeptide can be naturally occurring ("wild-type") or non-naturally occurring (e.g., a mutant, variant, etc.). Thus, a "recombinant" polypeptide is the result of human intervention, but may have a naturally occurring amino acid sequence.

[0072] In some embodiments, heteromultimers can be produced by a process in which host cells (e.g., Chinese hamster ovary cells) containing one or more nucleic acid sequences encoding a first heterodimer (that binds DLL3) and / or a second heterodimer (that binds CD3) described herein are cultured under conditions that allow expression of the heteromultimer, and then the expressed heteromultimer is recovered from the cell culture.

[0073] Methods for inhibiting DLL3-expressing cancers The present disclosure also provides a method of inhibiting the proliferation of DLL3-expressing cancer cells, comprising contacting a population of DLL3-expressing cancer cells and CD3-expressing T cells with an effective amount of a heteromultimer, or a composition comprising the heteromultimer, as described above. In some embodiments, a population of DLL3-expressing cancer cells and CD3-expressing T cells can be contacted with the heteromultimer, or a composition comprising the same, ex vivo, in vivo, or in vitro. "Ex vivo" refers to a method carried out in or on a cell or tissue in an artificial environment outside of an organism, with minimal modification of the natural conditions. In contrast, the term "in vivo" refers to a method carried out in an organism in its normal, intact state, while an "in vitro" method is carried out with components of the organism that have been isolated from the organism's usual biological context.

[0074] For any of the methods of treating cancer cells described herein, the cancer cells desirably express DLL3 on the cell surface. In some embodiments, cell surface expression of DLL3 protein can be determined by immunohistochemistry (IHC) or positron emission tomography (PET). For example, at least 5% (e.g., 5%, 10%, or 20%) of the cells of the cancer can be positive for DLL3 as determined by IHC. Any suitable IHC assay for determining DLL3 protein expression can be used in conjunction with the present disclosure. Desirably, the IHC assay is approved by a regulatory agency such as the US Food and Drug Association (FDA) or the European Medicines Agency (EMA). DLL3-specific IHC assays, and components thereof, are known in the art and commercially available from a variety of sources. For example, DLL3 expression in cancer or tumor cells can be detected using the VENTANA® DLL3 (SP347) Assay (Roche Diagnostics, GmbH, Mannheim, Germany). Other anti-DLL3 antibodies that can be used to detect DLL3 expression in an IHC assay include, but are not limited to, NBP2-24669 (Novus Biological, Littleton, CA); PA5-26336 (Thermo Fisher Scientific, Waltham, MA); and ab229902 (Abcam, Cambridge, MA). Exemplary PET assays for determining DLL protein expression are described in Chou et al., Cancer Res (2023) 83(2): 301-315; Sharma et al., Cancer Res. 2017 July 15; 77(14): 3931-3941. Doi: 10.1158 / 0008-5472. CAN-17-0299; and Poirier, JT, Journal of Thoracic Oncology Vol. 15 No. 2S (2020).Expression of DLL3 mRNA can be determined using methods known in the art, such as, for example, flow cytometry-based methods, polymerase chain reaction (PCR) analysis, sequencing analysis (e.g., RNA sequencing), electrophoretic analysis, restriction fragment length polymorphism (RFLP) analysis, Northern blot analysis, quantitative PCR, reverse transcriptase-PCR analysis (RT-PCR), and the like.

[0075] In exemplary aspects of the methods described herein, the heteromultimer also binds to human CD3 expressed on the surface of T cells. As explained above, CD3 associates with the T cell receptor to form a T cell receptor complex, which results in the generation of an activation signal in the T lymphocyte. In some embodiments, the second heterodimer comprises heavy and light chain polypeptides comprising CD3-binding amino acid sequences designated "I2E" or "I2E2", the sequences of which are set forth in the sequence listing below.

[0076] Any suitable type of cancer cell may be contacted with the heteromultimer or composition described herein. In certain embodiments, the cancer is a neuroendocrine cancer. Neuroendocrine cancer or tumor (NEC or NEN) is a relatively rare, heterogeneous tumor type that accounts for approximately 2% of all malignancies and affects less than 200,000 people in the United States (Oronsky et al., Neoplasia, 19(12):991-1002 (2017)). The term "neuroendocrine" applies to a wide variety of cells that have "endocrine" properties similar to those of nerve cells, such as the presence of dense-core granules (DCGs4) similar to those present in serotonergic neurons that store monoamines, and the synthesis and secretion of these monoamines. The neuroendocrine (NE) system includes endocrine glands, such as the pituitary gland, parathyroid gland, and NE adrenal gland, as well as endocrine pancreatic islet tissue embedded in glandular tissue (thyroid or pancreatic gland) and scattered cells in the exocrine parenchyma, such as endocrine system cells of the digestive tract and airway, which belong to what is known as the diffuse endocrine system. Most neuroendocrine tumors arise in the lung, appendix, small intestine, rectum, and pancreas. Neuroendocrine cancers include, but are not limited to, small cell lung cancer (SCLC), neuroendocrine prostate cancer (NEPC), and neuroblastoma.

[0077] In some embodiments, the tumor or cancer is lung cancer, such as SCLC or non-small cell lung cancer (NSCLC), glioma, glioblastoma, melanoma, prostate cancer, such as NEPC, neuroendocrine pancreatic cancer, hepatoblastoma, large cell lung neuroendocrine carcinoma, pancreatic neuroendocrine carcinoma, bladder neuroendocrine carcinoma, gastric neuroendocrine carcinoma, adrenal exocrine tumor, Merkel cell carcinoma, neuroblastoma, head and neck carcinoid or neuroendocrine carcinoma, head and neck paraganglioma, or cervical small cell neuroendocrine carcinoma. In some embodiments, the tumor or cancer is neuroendocrine prostate cancer.

[0078] In an exemplary embodiment, the cancer is histologically or cytologically confirmed SCLC. Optionally, the SCLC is measurable by modified Response Criteria in Solid Tumors (RECIST) 1.1, where measurable lesions include (a) non-nodal lesions with clear borders that can be precisely and continuously measured in one dimension of the axial plane (longest diameter ≧10 mm as measured by magnetic resonance imaging / computed tomography (MRI / CT) with a scan slice thickness ≦5 mm) and / or (b) nodal lesions with longest diameter ≧15 mm perpendicular to the long (short) axis on MRI / CT, ​​and / or exclude simple cysts, pleural / pericardial effusions, and ascites.

[0079] In embodiments where the cancer cells are in vivo, the present disclosure provides a method of treating a DLL3-expressing cancer in a subject in need thereof, comprising administering to the subject an effective amount of a heteromultimer described herein, or a composition comprising a heteromultimer. The present disclosure also provides the use of the heteromultimer in the manufacture of a medicament for the treatment of a DLL3-expressing cancer. As explained above, the cancer may be a neuroendocrine cancer, including, but not limited to, SCLC, NEPC, or neuroblastoma.

[0080] The term "treatment" includes preventative treatment and / or therapeutic treatment. Treatment is considered to be preventative treatment when administered prior to clinical signs of a condition. Therapeutic treatment includes, for example, amelioration or reduction of disease severity or shortening of disease duration. Additionally, the term "treat" and related terms do not necessarily mean 100% or complete treatment. Rather, there are various degrees of treatment that one of skill in the art recognizes as having potential benefits or therapeutic effects. In this regard, the method of treating cancer of the present disclosure can provide any amount or level of treatment. Additionally, the treatment provided by the method of the present disclosure can include treatment of one or more pathologies or symptoms or signs of the cancer being treated. Additionally, the treatment provided by the method of the present disclosure can include slowing the progression of the cancer. For example, the method can treat cancer by enhancing T cell activity or immune response against the cancer, reducing tumor or cancer growth, reducing metastasis of tumor cells, increasing cell death of tumor or cancer cells, etc. In exemplary embodiments, the method may delay the onset or recurrence of cancer for at least about 30 days, 2 months, 4 months, 6 months, 1 year, 2 years, 4 years, or more. In exemplary embodiments, the treatment may include extending the subject's survival. In various embodiments, the treatment provided by the methods of the present disclosure includes a therapeutic response according to Response Evaluation Criteria in Solid Tumors (RECIST) or other similar criteria. RECIST is a set of criteria for evaluating the progression, stabilization, or response of tumors and / or cancer cells, jointly developed by the National Cancer Institute of the United States, the National Cancer Institute of Canada Clinical Trials Group, and the European Organisation for Research and Treatment of Cancer.

[0081] The therapeutic effect can be monitored by periodic evaluation of the patient being treated. In the case of repeated administration over several days or longer, depending on the condition, the treatment can be repeated until a desired suppression of disease symptoms is observed. However, other dosage regimens may be useful and are within the scope of the present disclosure.

[0082] As explained above, the disclosed heteromultimers, or compositions comprising the heteromultimers, can be administered to a subject using standard administration techniques, including oral, intravenous, intraperitoneal, subcutaneous, pulmonary, transdermal, subcutaneous, intramuscular, intranasal, buccal, sublingual, or suppository administration. The desired dosage can be delivered by a single bolus of the composition, by multiple bolus administrations of the composition, by continuous infusion of the composition, or by any combination of the above administration methods.

[0083] In some embodiments of the methods disclosed herein, the heteromultimers or compositions may be administered alone (i.e., as a "monotherapy") or in combination with at least one additional therapeutic agent to achieve a desired biological effect in a subject. In an exemplary aspect, the at least one additional therapeutic agent may be a cancer therapy. The choice of cancer therapy used in combination with the disclosed methods depends on a variety of factors, including the cancer / tumor type, the stage and / or grade of the tumor or cancer, the age of the subject, and the like. Suitable cancer treatments that may be used include, but are not limited to, surgery, chemotherapy, radiation therapy, targeted therapy, immunotherapy, hormone therapy, and stem cell transplantation.

[0084] In some embodiments, the at least one additional therapeutic agent may be a chemotherapeutic agent. "Chemotherapeutic agents," also referred to as anti-neoplastic agents, include compounds useful in the treatment of cancer. Chemotherapeutic agents can be classified according to their mechanism of action and can be further divided into subgroups within each class. Exemplary classes of chemotherapeutic agents include alkylating agents, antimetabolites, topoisomerase inhibitors, antitumor antibiotics, mitotic inhibitors, and protein kinase inhibitors. Alkylating agents include subgroups such as oxazaphosphorines, nitrogen mustards, imidazotetrazines, nitrosoureas, alkylsulfonates, hydrazines, and platinum-based agents. Platinum-based agents include cisplatin, carboplatin, and oxaliplatin. Topoisomerase inhibitors include topoisomerase I inhibitors and topoisomerase II inhibitors. Mitotic inhibitors include vinca alkaloids, taxanes, and nontaxane microtubule inhibitors. Antitumor antibiotics include bleomycin, actinomycin D (dactinomycin), and mitomycin.

[0085] In certain embodiments, the chemotherapeutic agent that can be used in the methods disclosed herein is an alkylating agent. In an exemplary embodiment, the alkylating agent can be a platinum-based agent, such as cisplatin, carboplatin, or oxaliplatin. In certain embodiments, the alkylating agent is lurbinectedin (ZEPZELCA™). In other embodiments, the chemotherapeutic agent can be a topoisomerase inhibitor, such as a topoisomerase II inhibitor (e.g., etoposide). In certain embodiments, the chemotherapeutic agent that can be used in the methods disclosed herein includes a platinum-based agent (cisplatin, carboplatin, or oxaliplatin), a topoisomerase II inhibitor (etoposide), or a combination of a platinum-based agent and a topoisomerase II inhibitor.

[0086] In other embodiments, the at least one additional therapy can be a targeted cancer therapy (also referred to as "precision oncology therapy"). Exemplary targeted cancer therapies include, but are not limited to, protein kinase inhibitors (e.g., BCR-ABL and c-KIT tyrosine kinase inhibitors, EGFR tyrosine kinase inhibitors, ALK tyrosine kinase inhibitors, V600E mutant BRAF oncogene inhibitors, MEK inhibitors, Bruton's kinase inhibitors, Janus kinase inhibitors, and CDK inhibitors).

[0087] In other exemplary embodiments, the at least one additional therapeutic agent may be a programmed cell death 1 (PD-1) / programmed cell death ligand 1 (PD-L1) antagonist. PD-1, also known as CD279, SLEB2, and hSLE1, is a transmembrane protein expressed on activated T cells, natural killer (NK) cells and B lymphocytes, macrophages, dendritic cells (DCs), and monocytes. In particular, PD-1 is highly expressed on tumor-specific T cells (Han et al., Am J Cancer Res 10(3):727-742(2020)). PD-1 binds to B7 protein family members, programmed death (PD) ligand 1 (PD-L1; also known as CD274 and B7-H1), and PD ligand 2 (also known as PD-L2, CD273, and B7-DC). PD-L1 is constitutively expressed on T and B cells, macrophages, and dendritic cells, whereas PD-L2 expression is typically restricted to activated DCs and macrophages (Xing et al., Oncoimmunology 7(3):e1356144(2017)(doi:10.1080 / 2162402X.2017.1356144)). PD-1 inhibits both adaptive and innate immune responses.

[0088] The PD-1 / PD-L1 axis is involved in suppressing T cell immune responses in cancer. Antagonists of this pathway have been clinically validated in many solid tumor indications. Antagonist anti-PD-1 and anti-PD-L1 antibodies have been approved by the US Food and Drug Administration (FDA) for the treatment of various cancers. In some embodiments, agents targeting PD-1 (e.g., PD-1 antagonists or inhibitors) and / or agents targeting PD-L1 (e.g., PD-L1 antagonists or inhibitors) can be used in the methods disclosed herein to treat DLL3-expressing cancers. Exemplary agents targeting PD-1 include, but are not limited to, anti-PD-1 antibodies such as nivolumab, pembrolizumab, and cemiplimab. Exemplary agents targeting PD-L1 include, but are not limited to, anti-PD-L1 antibodies such as atezolizumab, avelumab, and durvalumab.

[0089] In a specific embodiment, the anti-PD-L1 antibody is atezolizumab (International Nonproprietary Name (INN) for Pharmaceutical Substances, WHO Drug Information, Vol. 29, No. 3, 2015, Recommended INN: List 74). Atezolizumab is a humanized PD-L1 blocking antibody. It is an immunoglobulin G1-κ, anti-[Homo sapiens CD274 (Programmed Death Ligand 1, PDL1, PD-L1, B7 Homolog 1, B7H1)], humanized monoclonal antibody; gamma 1 heavy chain (1-448) [humanized VH (Homo sapiens IGHV3-23 * 04(86.70%)-(IGHD)-IGHJ4 * 01) [8.8.11] (1-118) - Homo sapiens IGHG1 *03 (CH1 R120>K(215)(119-216), hinge(217-231), CH2 N84.4>A(298)(232-341), CH3(342-446), CHS(447-448))(119-448)], with κ light chain (221-214')-disulfide(1'-214') [humanized V-κ (Homo sapiens) IGKV1-5 * 01(87.90%)-IGKJ1 * 01) [6.3.9] (1'-107') - Homo sapiens IGKC * 01(108'-214')]; dimer (227-227":230-230")-bis ​​disulfide. Atezolizumab is commercially available, for example as TECENTRIQ®.

[0090] In a particular embodiment, the anti-PD-L1 antibody is avelumab (International Nonproprietary Name (INN) for Pharmaceutical Substances, WHO Drug Information Vol. 30, No. 1, 2016, Recommended INN: List 75). Avelumab is a PD-L1 blocking monoclonal antibody produced in CHO cells. It is composed of immunoglobulin G1-lambda1, anti-[Homo sapiens CD274 (Programmed Death Ligand 1, PDL1, PD-L1, B7 Homolog 1, B7H1)], Homo sapiens monoclonal antibody; gamma1 heavy chain (1-450) [Homo sapiens VH (IGHV3-23 * 01(90.80%)-(IGHD)-IGHJ4 * 01)[8.8.13](1-120)-IGHG1 * 01, Gm17, 1 (CH1(121-218), hinge(219-233), CH2(234-343), CH3(344-448), CHS(449-450)(121-450)], with λ1 light chain (223-215')-disulfide(1'-216') [Homo sapiens V-λ (IGLV2-14 * 01(99.00%)-IGLJ1 *01)[9.3.10](1'-110')-IGLC1 * 02(111'-216')]; dimer (229-229":232-232")-bis ​​disulfide. Avelumab is commercially available, for example as BAVENCIO®.

[0091] In a specific embodiment, the anti-PD-L1 antibody is durvalumab (International Nonproprietary Name (INN) for Pharmaceutical Substances, WHO Drug Information, Vol. 29, No. 3, 2015, Recommended INN: List 74). Durvalumab is a PD-L1 blocking monoclonal antibody produced in CHO cells. It is an immunoglobulin G1-κ, anti-[Homo sapiens CD274 (Programmed Death Ligand 1, PDL1, PD-L1, B7 Homolog 1, B7H1)], Homo sapiens monoclonal antibody; gamma 1 heavy chain (1-451) [Homo sapiens VH (IGHV3-7 * 01(99.00%)-(IGHD)-IGHJ4 * 01)[8.8.14](1-121)-IGHG1 * 03 (CH1(122-219), hinge(220-234), CH2(235-344) L1.3>F(238), L1.2>E(239), P116>S(335), CH3(345-449), CHS(450-451))(122-451)], with κ light chain (224-215')-disulfide(1'-215') [Homo sapiens V-κ (IGKV3-20 * 01(96.90%)-IGKJ1 * 01)[7.3.9](1'-108')-IGKC * 01(109'-215')]; dimer (230-230":233-233")-bis ​​disulfide. Durvalumab is commercially available, for example as IMFINZI®.

[0092] In various embodiments of the present disclosure, the subject is a human. In exemplary embodiments, the human subject has SCLC, optionally histologically or cytologically confirmed SCLC. In various embodiments, the human is male or female and / or is 18 years of age or older with SCLC. In exemplary embodiments, the human subject has relapsed / refractory (RR) SCLC that has progressed or relapsed after at least one platinum-based chemotherapy, optionally with or without a PD-L1 inhibitor. In exemplary embodiments, the human subject has ES-SCLC, optionally histologically or cytologically confirmed advanced stage SCLC (ES SCLC). In exemplary embodiments, the human subject has ES-SCLC and has not received prior systemic treatment for ES-SCLC. In exemplary embodiments, the human subject has an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1 (Oken et al., Am J Clin Oncol 5:649-655(1982)).

[0093] The following examples further illustrate the invention but, of course, should not be construed as in any way limiting its scope. EXAMPLES

[0094] Example 1 This example describes the generation of heteromultimers encompassed by the present disclosure.

[0095] A DLL3-targeting multichain T cell engager molecule (termed "mcTCE") was generated with three anti-DLL3 binding domains directed against diverse epitopes and a high affinity anti-CD3 binding domain. Hetero-IgG, AmAb ("Amgen monoclonal antibody"), NmAb (one scFv at the N-terminus of one Fab arm), and BmAb (one scFv between one Fab arm and the Fc portion) formats were generated (Figures 1A-1D) and evaluated for expression, purification, binding affinity, cell-based activity, immunogenic potential, pharmacokinetic profile, and physical and chemical stability.

[0096] In particular, on-cell binding affinity for DLL3 was assessed using Chinese Hamster Ovary (CHO) cells engineered to stably express either human or cynomolgus DLL3. Engineered CHO cells were incubated with DLL3 multichain TCE proteins containing two different DLL3 binders ("DLL3_1" or "DLL3_2") for 4 hours in buffer (phosphate buffered saline containing 1% fetal bovine serum). After incubation, cells were washed in buffer and then bound DLL3 multichain proteins were detected by incubation with a fluorescently labeled antibody against the fragment crystallizable (Fc) region of the protein. Bound proteins were analyzed by flow cytometry and EC 50 Values ​​were calculated from nonlinear regression analysis using GraphPad Prism, and the results are shown in Table 1.

[0097] [Table 1]

[0098] CD3 binding affinity was evaluated using surface plasmon resonance. CD3ε fusion protein (CD3ε (aa 1-27)-chicken albumin) was immobilized on CM5 Sensor Chips in the presence of sodium acetate buffer (pH 4.5). The above DLL3 multichain TCE protein diluted in HBS-EP buffer was applied at various concentrations to determine the molecular association rate with CD3ε. Then, HBP-EP buffer alone was added to allow the analysis of molecular association rate. Binding affinity calculations were performed using BiaEval software and the results are shown in Table 2.

[0099] [Table 2]

[0100] Cytotoxicity was evaluated using a T-cell-dependent cytotoxicity (TDCC) assay. For this purpose, unstimulated human peripheral blood mononuclear cells (PBMC; CD14- / CD56-) were co-cultured with target cells (CHO cells (non-transfected or stably expressing human DLL3), or small cell lung cancer cell lines SHP-77 or NCI-H82) at an effector to target cell (E:T) ratio of 10:1 and incubated with a range of concentrations of DLL3 multichain TCE protein for 48 hours. Cynomolgus T cell line LnPx4119 was co-cultured with CHO cells or CHO cells expressing cynomolgus DLL3 at a ratio of 10:1 and incubated with a range of concentrations of DLL3 multichain TCE molecules for 48 hours. T cell-dependent cytotoxicity was measured using a flow cytometry-based assay, in which target cells were pre-labeled with DiO-labeled dye (to mark live cells) and stained with propidium iodide (to mark dead cells) after 48 hours of incubation. Data was analyzed by nonlinear regression in GraphPad Prism and is shown in Table 3. DLL3_1 and DLL3_2 multimers in hetero-IgG format showed favorable cellular potency.

[0101] [Table 3]

[0102] The DLL3_1 and DLL3_2 hetero-IgG molecules also demonstrated antibody-like pharmacokinetic profiles (9.7-15.2 days; Figures 2A-2B and 3) in transgenic mouse models, as well as acceptable physical and chemical stability. To mitigate the risks associated with potential thermal instability at residue N103 in the CD3 CDR, forms of DLL3_1 and DLL3_2 hetero-IgG containing alternative CD3-binding domains were tested and shown to have improved stability.

[0103] Example 2 This example describes an analysis of the productivity of DLL3-targeting hetero-IgG molecules encompassed by this disclosure.

[0104] A DLL3-specific heterodimer was generated according to the methods described herein. The heterodimer (also designated "DLL3_2") contains a DLL3-binding heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO:54 and a light chain amino acid sequence of SEQ ID NO:55, and a CD3-binding heterodimer comprising a heavy chain amino acid sequence of SEQ ID NO:56 and a light chain amino acid sequence of SEQ ID NO:57.

[0105] Briefly, cells were cultivated in a stirred tank bioreactor in a 15-day perfusion system using an alternating tangential flow (ATF) filtration system (Repligen, Waltham MA, USA) coupled to a polysulfone filter (Cytiva, Westborough, MA, USA) and a proprietary chemically defined medium. On day 12, the ATF filter was switched from a 30 kDa retaining membrane to a 750 kDa membrane that allowed product to pass through the membrane while the cells still remained in the bioreactor. The accumulated harvested cell culture fluid (HCCF) represents the product collected (XMF harvest) over a 3-day perfusion process using the 750 kDa membrane. The HCCF product (in g) was calculated by multiplying the HCCF titer (g / L) by the XMF harvest volume (L).

[0106] The equivalent or final total bioreactor titer is a calculation that represents the total reactor productivity, adjusted to the reactor volume. This number allows comparison across projects and scales. It was calculated by adding the final reactor product (g of product remaining in the bioreactor after perfusion and adjusted by the loaded cell volume) and the HCCF product (in g) and dividing by the reactor volume. This calculated combined titer is comparable to the titer measured in a conventional fed-batch bioreactor process.

[0107] Titer assay Affinity Protein A ultra-performance liquid chromatography (UPLC) was used to analyze the concentration of CHO-expressed recombinant heterologous IgG protein in conditioned media such as XMF harvests.

[0108] Briefly, it uses affinity chromatography where Protein A is immobilized on a column support. At neutral pH, CHO-expressed hetero-IgG binds to Protein A via the Fc region, while host cell proteins (HCPs), conditioned medium components, and buffer are not retained and are eluted from the column in the flow-through. Capture mAb and CHO-expressed Fc-fusion proteins are eluted at acidic pH and detected by UV absorbance at 280 nm. Calibration curves are derived from mAb or CHO-expressed Fc-fusion protein standards and the corresponding peak areas using linear regression analysis.

[0109] Yield calculation The harvest yield (in %) or XMF harvest yield was calculated by dividing the amount of HCCF product (in g) by the total products combined (in g).

[0110] The purification yield is the sum of the yields of all steps in the purification workflow. In this specification, the purification yield represents the sum of the step yields from Protein A capture, cation exchange chromatography (CEX), multi-module process (MMC), viral filtration, and the final ultrafiltration / diafiltration (UF / DF) concentration and formulation steps.

[0111] The total yield is a combination of the XMF harvest and purification yields. It represents the ratio of final drug substance (DS) (in g) over the total product (in g) combined.

[0112] Final predicted productivity (in g DS / L bioreactor volume) is the result of the final total bioreactor titer (g / L) along with total yield (in %). Productivity, titer, and yield of DLL3_2 single cell clones compared to AMG 757 (tarlatamab) are shown in Table 4. As described herein, AMG 757 is a DLL3-specific half-life extended (HLE) BiTE® molecule developed for the treatment of SCLC. Surprisingly, the yield of drug substance per L bioreactor volume of DLL3_2 (2.7 g / L) was 270% higher than AMG 757.

[0113] [Table 4]

[0114] Example 3 This example describes the molecular characterization of the DLL3-targeting hetero-IgG molecules encompassed by this disclosure.

[0115] Biochemical, biophysical, and biological characterization of DLL3#2 was performed at various stages of downstream production to provide a comprehensive understanding of its structural and functional properties and allow for the evaluation of attributes that may affect binding and efficacy (e.g., aggregation, high molecular weight (HMW) species, and charge variants). For example, visible particles present in platform DLL3#2 formulations were assessed by visual inspection; high molecular weight species were assessed by size exclusion chromatography (SEC); low molecular weight species were assessed by rCE-SDS (reduced capillary electrophoresis-sodium dodecyl sulfate); charge variants were assessed by CEX-UPLC (cation exchange ultra-performance liquid chromatography); chemical modifications to DLL3#2 were assessed by peptide mapping; subvisible particles were assessed by HAIC (high accuracy liquid particle counter) and / or BMI (background membrane imaging); protein concentration / recovery was determined by SPR (surface plasmon resonance). IV compatibility studies and agitation evaluations were also performed.

[0116] CEX-UPLC evaluation showed slightly increased acidic and basic peak levels after the second Photo Stress (P2) and increased acidic and basic peak levels after storage of the platform formulation of DLL3#2 at 40° C. An increase in HMW was observed after P2 and after storage at 40° C. There was no increase in HMW after storage at −20° C. and after freeze-thaw.

[0117] rCE-SDS analysis showed increased polypeptide clipping after storage at 40°C; however, changes in LMW (<5%) after 4 weeks of storage at 40°C were within the defined quality profile.

[0118] The titers, HMW species, LMW species, and charge variants of the amplified pools of DLL3_2 were compared to other DLL3-specific heterodimeric IgG molecules (A, B, and C), as well as to a representative BiTE®-HLE molecule. Table 5 shows that the average titers of the amplified DLL3_2 pools were 2-3 times higher than for the pools of BiTE®-HLE molecules, and that the individual DLL3 TCE heterodimeric IgG pools have significantly improved titers and product quality compared to the BiTE-HLE pools. Thus, DLL3-specific heterodimeric multimers encompassed by the present disclosure, including DLL3_2, have advantageous manufacturing properties compared to conventional BiTE® molecules.

[0119] [Table 5]

[0120] Example 4 This example describes an exploratory single-dose pharmacokinetic and local tolerance study of a DLL3-targeted hetero-IgG molecule in cynomolgus monkeys.

[0121] Quantification of DLL3_2 (above) in cynomolgus monkey serum was performed using three electrochemiluminescence immunoassays using 1) biotinylated anti-CD3 monoclonal antibody (MAb) as capture reagent and ruthenylated mouse anti-human IgG Fc MAb as detection reagent (assay-1), 2) biotinylated human DLL3 (R&D Systems, Cat# 9749-DL) as capture reagent and ruthenylated mouse anti-human IgG Fc MAb as detection reagent (assay-2), and 3) biotinylated mouse anti-human IgG Fc MAb as capture reagent and ruthenylated mouse anti-human IgG Fc MAb as detection reagent (assay-3). Analyte serum concentrations were interpolated from the standard curve using the corresponding analyte. The lower limit of quantification (LLOQ) of the assay in serum was 0.61 ng / ml, while the upper limit of quantification (ULOQ) of the assay in serum was 10000 ng / mL in all formats.

[0122] Toxicokinetic analysis was performed and data for TK analysis was extracted from the non-GLP Watson database into PHOENIX®. Noncompartmental analysis (NCA) was performed on individual serum concentration-nominal time data from 0 to 168 hours post-dose using PHOENIX® WINNONLIN® (version 6.4). The following PK parameters were estimated: max (maximum concentration in serum), AUC 0-336 (area under the concentration-time curve from time 0 to 336 hours after dosing, estimated by the linear trapezoidal method).

[0123] All three assay formats resulted in similar serum concentrations of the administered molecules, indicating that there was no significant clipping of the molecules in serum over the course of the experiment. A rapid decrease in serum concentration of the administered molecules was observed after 336 hours. This decrease in serum concentration may be due to the possible generation of anti-drug antibodies (ADAs). These ADAs may have resulted in a faster clearance of the administered molecules or may have interfered with either the capture or detection reagents inhibiting the detection of the administered molecules.

[0124] DLL3_2 showed good serum exposure when administered either subcutaneously or intravenously, as shown in Figures 4A and 4B. Bioavailability of DLL3_2 in Cynomolgus Monkeys [(mean AUC SC / Administration SC ) / (average AUC IV / Administration IV ) was 93.6%, indicating good release of DLL3_2 into the circulation from the subcutaneous administration site.

[0125] All references cited in this specification, including publications, patent applications, and patents, are herein incorporated by reference to the same extent as if each reference was individually and specifically indicated to be incorporated by reference and was set forth in its entirety herein.

[0126] Use of the terms "a," "an," "the," and "at least one" and similar referents with respect to the description of the invention (especially with respect to the claims below) should be construed to encompass both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The term "at least one" followed by a list of one or more items (e.g., "at least one of A and B") should be construed to mean one item (A or B) selected from the listed items or any combination of two or more of the listed items (A and B), unless otherwise indicated herein or clearly contradicted by context. The terms "comprising," "having," "including," and "containing" should be construed as open-ended terms (i.e., meaning "including, but not limited to"), unless otherwise indicated herein. The recitation of ranges of values ​​herein is intended to serve as a shorthand method of referring individually to each separate value falling within the range, and each separate value is incorporated herein as if it were individually recited herein, unless otherwise indicated herein. All of the methods described herein may be performed in any suitable order, unless otherwise indicated herein or clearly contradicted by context. The use of any examples or exemplary language (e.g., "etc.") provided herein is merely intended to further clarify the invention, and does not impose limitations on the scope of the invention unless otherwise asserted. No language in the specification should be construed as indicating any non-claimed element as essential to the practice of the invention.

[0127] Preferred embodiments of the invention are described herein, including the best mode known to the inventors for carrying out the invention. Variations of those preferred embodiments may become apparent to those of ordinary skill in the art upon reading the foregoing description. The inventors anticipate that those of ordinary skill in the art will employ such variations as necessary, and the inventors intend for the invention to be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents of the subject matter recited in the claims appended hereto as permitted by applicable law. Moreover, any combination of the above-described elements in all possible variations thereof is encompassed by the invention unless otherwise indicated herein or clearly contradicted by context.

[0128] [Table 6]

[0129] [Table 6A-1]

[0130] [Table 6A-2]

[0131] [Table 7]

[0132] [Table 7A-1]

[0133] [Table 7A-2]

[0134] [Table 8]

[0135]

Table 8A-1

[0136]

Table 8A-2

[0137]

Table 9

[0138]

Table 9A-1

[0139]

Table 9A-2

[0140]

Table 9A-3

[0141]

Table 10

[0142] [Table 10A]

[0143]

Table 11

[0144]

Table 11A

[0145]

Table 12-1

[0146]

Table 12-2

[0147]

Table 12A-1

[0148]

Table 12A-2

[0149]

Table 13-1

[0150]

Table 13-2

[0151]

Table 13-3

[0152]

Table 13A-1

[0153]

Table 13A-2

[0154]

Table 13A-3

[0155]

Table 13A-4

[0156]

Table 14-1

[0157]

Table 14-2

[0158]

Table 14-3

[0159]

Table 14-4

[0160]

Table 14-5

[0161]

Table 14-6

[0162]

Table 14-7

[0163]

Table 14-8

[0164]

Table 14-9

[0165]

Table 14A-1

[0166]

Table 14A-2

[0167]

Table 14A-3

[0168]

Table 14A-4

[0169]

Table 14A-5

[0170]

Table 14A-6

[0171]

Table 14A-7

Claims

1. A heteropolymer comprising a first heterodimer that binds to human delta-like ligand 3 (DLL3) and a second heterodimer that binds to human differentiation cluster (CD) 3 (CD3), (a) The first heterodimer comprises a heavy chain (HC) containing the amino acid sequence of SEQ ID NO: 54 or SEQ ID NO: 58; and a light chain (LC) containing the amino acid sequence of SEQ ID NO: 55 or SEQ ID NO: 59; (b) A heteropolymer comprising a heavy chain containing the amino acid sequence of SEQ ID NO: 56 or SEQ ID NO: 132, and a light chain containing the amino acid sequence of SEQ ID NO:

57.

2. The heteropolymer according to claim 1, wherein the first heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 54 and a light chain containing the amino acid sequence of SEQ ID NO:

55.

3. The heteropolymer according to claim 1, wherein the first heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 58 and a light chain containing the amino acid sequence of SEQ ID NO:

59.

4. The heteropolymer according to any one of claims 1 to 3, wherein the second heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 56 and a light chain containing the amino acid sequence of SEQ ID NO:

57.

5. The heteropolymer according to any one of claims 1 to 3, wherein the second heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 132 and a light chain containing the amino acid sequence of SEQ ID NO:

57.

6. (a) The first heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 54 and a light chain containing the amino acid sequence of SEQ ID NO: 55; (b) The heteropolymer according to claim 1, wherein the second heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 56 and a light chain containing the amino acid sequence of SEQ ID NO:

57.

7. (a) The first heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 54 and a light chain containing the amino acid sequence of SEQ ID NO: 55; (b) The heteropolymer according to claim 1, wherein the second heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 132 and a light chain containing the amino acid sequence of SEQ ID NO:

57.

8. (a) The first heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 58 and a light chain containing the amino acid sequence of SEQ ID NO: 59; (b) The heteropolymer according to claim 1, wherein the second heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 56 and a light chain containing the amino acid sequence of SEQ ID NO:

57.

9. (a) The first heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 58 and a light chain containing the amino acid sequence of SEQ ID NO: 59; (b) The heteropolymer according to claim 1, wherein the second heterodimer comprises a heavy chain containing the amino acid sequence of SEQ ID NO: 132 and a light chain containing the amino acid sequence of SEQ ID NO:

57.

10. The heteromultimer according to claim 1, wherein the first heterodimer binds to human DLL3 expressed on the surface of a target cell.

11. The heteromultimer according to claim 10, wherein the target cell is a cancer cell.

12. The heteromultimer according to claim 11, wherein the cancer cells are neuroendocrine carcinoma cells.

13. The heteromultimer according to claim 12, wherein the neuroendocrine carcinoma is small cell lung cancer (SCLC) or neuroendocrine prostate cancer (NEPC).

14. The heteromultimer according to any one of claims 1 to 3 or 6 to 13, wherein the second heterodimer binds to human CD3 expressed on the surface of T cells.

15. A composition comprising a heteropolymer according to any one of claims 1 to 3 or 6 to 13 and a pharmaceutically acceptable carrier.

16. A kit comprising the composition and instructions for use described in claim 15.

17. A composition for use in a method for inhibiting the proliferation of DLL3-expressing cancer cells, comprising a heteromultimer according to any one of claims 1 to 3 or 6 to 13 and a pharmaceutically acceptable carrier, wherein the method comprises contacting a population of DLL3-expressing cancer cells and CD3-expressing T cells with the heteromultimer or the composition.

18. The composition according to claim 17, characterized in that the populations of DLL3-expressing cancer cells and CD3-expressing T cells are contacted in vitro.

19. The composition according to claim 17, characterized in that the populations of DLL3-expressing cancer cells and CD3-expressing T cells are contacted in vivo.

20. A composition for use in a method for treating DLL3-expressing cancer in a subject requiring treatment for DLL3-expressing cancer, comprising a heteromultimer according to any one of claims 1 to 3 or 6 to 13 and a pharmaceutically acceptable carrier, wherein the method comprises administering the heteromultimer or the composition to the subject.

21. The composition according to claim 20, wherein the cancer is neuroendocrine carcinoma.

22. The composition according to claim 21, wherein the neuroendocrine carcinoma is small cell lung cancer (SCLC) or neuroendocrine prostate cancer (NEPC).

23. The composition according to claim 20, characterized in that the heteropolymer or composition is administered intravenously, intramuscularly, or subcutaneously to the subject.

24. The composition according to claim 20, wherein the method further comprises administering at least one further therapeutic agent to the subject.

25. The composition according to claim 24, wherein the further therapeutic agent comprises one or more chemotherapeutic agents or programmed cell death 1 (PD-1) / programmed cell death ligand 1 (PD-L1) antagonists.

26. The composition according to claim 25, wherein the PD-1 / PD-L1 antagonist is an anti-PD-1 antibody or an anti-PD-L1 antibody.

27. The composition according to claim 26, wherein the anti-PD-1 antibody comprises nivolumab, pembrolizumab, or semiprimab.

28. The composition according to claim 26, wherein the anti-PD-L1 antibody comprises atezolizumab, avelumab, or durvalumab.

29. The composition according to claim 25, wherein the one or more chemotherapeutic agents include an alkylating agent, a platinum-based chemotherapeutic agent, etoposide, or any combination thereof.

30. The composition according to claim 29, wherein the alkylating agent is lurubinectedin.

31. The composition according to claim 29, wherein the platinum-based chemotherapeutic agent is carboplatin or cisplatin.

32. The composition according to claim 20, wherein the subject is a human.

33. A nucleic acid sequence encoding a heteromultimer according to any one of claims 1 to 3 or 6 to 13.

34. Use of a heteropolymer according to any one of claims 1 to 3 or 6 to 13 in the manufacture of a drug for the treatment of DLL3-expressing cancer.

35. The use according to claim 34, wherein the cancer is neuroendocrine carcinoma.

36. The use according to claim 35, wherein the neuroendocrine carcinoma is small cell lung cancer (SCLC), neuroendocrine prostate cancer (NEPC), or neuroblastoma.

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