Antibody molecules to CD138 and uses thereof

US11945868B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11945868-B2
Application numberUS-201816149854-A
CountryUS
Kind codeB2
Filing dateOct 2, 2018
Priority dateOct 2, 2017
Publication dateApr 2, 2024
Grant dateApr 2, 2024

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Antibody molecules that specifically bind to CD138 are disclosed. The antibody molecules can be used to treat, prevent, and/or diagnose disorders, such as multiple myeloma.

First claim

Opening claim text (preview).

What is claimed is: 1. An anti-CD138 antibody molecule comprising: (a) a heavy chain variable region (VH), wherein the VH comprises three heavy chain complementarity determining regions (HCDR1, HCDR2, and HCDR3), wherein the VH comprises: (i) an HCDR1 comprising the amino acid sequence of SEQ ID NO: 350, 355, or 356, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 351, and an HCDR3 comprising the amino acid sequence of FVY; or (ii) an HCDR1 comprising the amino acid sequence of SEQ ID NO: 380, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 381 or 382, and an HCDR3 comprising the amino acid sequence of FVY; and (b) a light chain variable region (VL), wherein the VL comprises three light chain complementarity determining regions (LCDR1, LCDR2, and LCDR3), wherein the VL comprises: an LCDR1 comprising the amino acid sequence of SEQ ID NO: 352 or an amino acid sequence that differs by 1 conservative amino acid substitution therefrom; an LCDR2 comprising the amino acid sequence of SEQ ID NO: 353; and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 354. 2. The antibody molecule of claim 1 , which is a synthetic antibody molecule, a humanized antibody molecule, or an isolated antibody molecule, and/or is a monovalent antibody molecule, a multivalent antibody molecule, a monospecific molecule, or a multispecific antibody molecule. 3. The antibody molecule of claim 1 , comprising a heavy chain constant region of IgG chosen from IgG1, IgG2, IgG3, or IgG4, and/or a light chain constant region of kappa or lambda light chain. 4. The antibody molecule of claim 1 , comprising an Fc region comprising one or more mutations that increases the binding affinity to neonatal receptor FcRn and/or the half-life of the antibody molecule. 5. An antibody-molecule drug conjugate (ADC) comprising an antibody molecule of claim 1 . 6. A pharmaceutical composition comprising an antibody molecule of claim 1 and a pharmaceutically acceptable carrier. 7. A nucleic acid molecule encoding a heavy chain variable region (VH), a light chain variable region (VL), or both, of an antibody molecule of claim 1 . 8. A vector comprising a nucleic acid molecule of claim 7 . 9. A cell comprising a nucleic acid molecule of claim 7 . 10. A kit comprising an antibody molecule of claim 1 and instructions to use of the antibody molecule or composition. 11. A container comprising an antibody molecule of claim 1 . 12. A method of producing an anti-CD138 antibody molecule, the method comprising culturing a cell of claim 9 under conditions that allow production of an antibody molecule, thereby producing the antibody molecule. 13. A method of causing an ADCC activity, the method comprising contacting a CD138-expressing cell or a subject comprising said cell with an antibody molecule of claim 1 , thereby causing the ADCC activity. 14. A method of treating a CD138-expressing cancer, the method comprising administering to a subject in need thereof an effective amount of an antibody molecule of claim 1 , thereby treating the CD138-expressing cancer. 15. The method of claim 14 , wherein the CD138-expressing cancer is a myeloma. 16. A method of treating a CD138-expressing precancerous condition, the method comprising administering to a subject in need thereof an effective amount of an antibody molecule of claim 1 , thereby treating the CD138-expressing precancerous condition. 17. The method of claim 16 , wherein the CD138-expressing precancerous condition is smoldering myeloma or monoclonal gammopathy of undetermined significance (MGUS). 18. A method of detecting a CD138 molecule, the method comprising contacting a cell or a subject with an antibody molecule of claim 1 , thereby detecting the CD138 molecule. 19. The antibody molecule of claim 1 , wherein the VH comprises an HCDR1 comprising the amino acid sequence of SEQ ID NO: 350, 355, or 356, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 351, and an HCDR3 comprising the amino acid sequence of FVY. 20. The antibody molecule of claim 1 , wherein the VH comprises an HCDR1 comprising the amino acid sequence of SEQ ID NO: 380, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 381 or 382, and an HCDR3 comprising the amino acid sequence of FVY. 21. The antibody molecule of claim 1 , wherein: (a) the VH comprises: an HCDR1 comprising the amino acid sequence of SEQ ID NO: 350, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 351, and an HCDR3 comprising the amino acid sequence of FVY; and (b) the VL comprises: an LCDR1 comprising the amino acid sequence of SEQ ID NO: 352 or an amino acid sequence that differs by 1 conservative amino acid substitution therefrom, an LCDR2 comprising the amino acid sequence of SEQ ID NO: 353, and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 354. 22. The antibody molecule of claim 1 , wherein: (a) the VH comprises: an HCDR1 comprising the amino acid sequence of SEQ ID NO: 355, an HCDR2 comprising the amino acid sequence of SEQ ID NO: 351, and an HCDR3 comprising the amino acid sequence of FVY; and (b) the VL comprises: an LCDR1 comprising the amino acid sequence of SEQ ID NO: 352 or an amino acid sequence that differs by 1 conservative amino acid substitution therefrom, an LCDR2 comprising the amino acid sequence of SEQ ID NO: 353, and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 354. 23. The antibody molecule of claim 1 , wherein: (a) the VH comprises: an HCDR1 comprising an amino acid sequence comprising the amino acid sequence of SEQ ID NO: 356, an HCDR2 comprising an amino acid sequence comprising the amino acid sequence of SEQ ID NO: 351, and an HCDR3 comprising the amino acid sequence of FVY; and (b) the VL comprises: an LCDR1 comprising the amino acid sequence of SEQ ID NO: 352 or an amino acid sequence that differs by 1 conservative amino acid substitution therefrom, an LCDR2 comprising the amino acid sequence of SEQ ID NO: 353, and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 354. 24. The antibody molecule of claim 1 , wherein: (a) the VH comprises: an HCDR1 comprising an amino acid sequence comprising the amino acid sequence of SEQ ID NO: 380, an HCDR2 comprising an amino acid sequence comprising the amino acid sequence of SEQ ID NO: 381, and an HCDR3 comprising the amino acid sequence of FVY; and (b) the VL comprises: an LCDR1 comprising the amino acid sequence of SEQ ID NO: 352 or an amino acid sequence that differs by 1 conservative amino acid substitution therefrom, an LCDR2 comprising the amino acid sequence of SEQ ID NO: 353, and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 354. 25. The antibody molecule of claim 1 , wherein: (a) the VH comprises: an HCDR1 comprising an amino acid sequence comprising the amino acid sequence of SEQ ID NO: 380, an HCDR2 comprising an amino acid sequence comprising the amino acid sequence of SEQ ID NO: 382, and an HCDR3 comprising the amino acid sequence of FVY; and (b) the VL comprises: an LCDR1 comprising the amino acid sequence of SEQ ID NO: 352 or an amino acid sequence that differs by 1 conservative amino acid substitution therefrom, an LCDR2 comprising the amino acid sequence of SEQ ID NO: 353, and an LCDR3 comprising the amino acid sequence of SEQ ID NO: 354. 26. The antibody molecule of claim 1 , wherein the VH comprises an amino acid sequence that differs by no more than 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11,

Assignees

Inventors

Classifications

  • against CD28 or CD152 · CPC title

  • C07K16/28Primary

    against receptors, cell surface antigens or cell surface determinants · CPC title

  • Antibody-dependent cellular cytotoxicity [ADCC] · CPC title

  • cytotoxic response · CPC title

  • comprising antibodies · CPC title

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Frequently asked questions

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What does patent US11945868B2 cover?
Antibody molecules that specifically bind to CD138 are disclosed. The antibody molecules can be used to treat, prevent, and/or diagnose disorders, such as multiple myeloma.
Who is the assignee on this patent?
Visterra Inc
What technology area does this patent fall under?
Primary CPC classification C07K16/2818. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 02 2024 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 7 related publications on this page (citations in our corpus or others sharing the same primary CPC).