IP Library Granted Patent US 9,175,081
Granted Patent B2
US 9,175,081 · App. 13/894,857 · Granted Nov 3, 2015

Therapeutic use of anti-CS1 antibodies

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Quick Facts
Patent No.
US 9,175,081
App. No.
13/894,857
Granted
Nov 3, 2015
Kind
B2
Abstract

The present invention is directed to antagonists of CS1 that bind to and neutralize at least one biological activity of CS1. The invention also includes a pharmaceutical composition comprising such antibodies or antigen-binding fragments thereof. The present invention also provides for a method of preventing or treating disease states, including autoimmune disorders and cancer, in a subject in need thereof, comprising administering into said subject an effective amount of such antagonists.

Claims (36)

1. A method of treating myeloma, comprising administering to a patient suffering from myeloma but who has not developed clinical manifestations of myeloma, a therapeutically effective amount of a monoclonal anti-CS1 antibody or an anti-CS1 antigen binding fragment, wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment binds to a protein encoded by SEQ ID NO:1.

2. The method of claim 1 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment inhibits immunoglobulin secretion.

3. The method of claim 1 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is humanized.

4. The method of claim 1 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment induces antibody-dependent cellular cytotoxicity (“ADCC”) of cells expressing said protein encoded by SEQ ID NO:1.

5. The method of claim 4 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment induces at least 40% cytotoxicity of cells expressing said protein encoded by SEQ ID NO:1.

6. The method of claim 4 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment induces at least 60% cytotoxicity of cells expressing said protein encoded by SEQ ID NO:1.

7. The method of claim 1 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is an IgG 1 .

8. The method of claim 1 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment has a low level of or lacks fucose.

9. The method of claim 1 , further comprising administering to the patient an immunosuppressive drug.

10. The method of claim 1 , further comprising administering to the patient an immunodulator.

11. The method of claim 10 , further comprising administering to the patient an immunosuppressive drug.

12. The method of claim 9 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is administered after the immunosuppressive drug.

13. The method of claim 9 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is administered in combination with the immunosuppressive drug.

14. The method of claim 10 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is administered after the immunomodulator.

15. The method of claim 10 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is administered in combination with the immunomodulator.

16. The method of claim 11 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is administered after the immunosuppressive drug and the immunomodulator.

17. The method of claim 11 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is administered in combination with the immunosuppressive drug and the immunomodulator.

18. A method of treating myeloma, comprising administering to a patient suffering from myeloma but who has not developed clinical manifestations of myeloma, a therapeutically effective amount of a conjugate compound comprising a monoclonal anti-CS1 antibody or an anti-CS1 antigen binding fragment linked to an effector moiety, wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment binds to a protein encoded by SEQ ID NO:1.

19. The method of claim 18 , wherein the effector moiety is a cytotoxic agent.

20. The method of claim 18 , wherein the effector moiety is a detection moiety, an activatable moiety, a chemotherapeutic agent, a lipase, an antibiotic, a chemoattracting agent, an immune modulator or a radioisotope.

21. The method of claim 18 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment inhibits immunoglobulin secretion.

22. The method of claim 18 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is humanized.

23. The method of claim 18 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment induces antibody-dependent cellular cytotoxicity (“ADCC”) of cells expressing said protein encoded by SEQ ID NO:1.

24. The method of claim 23 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment induces at least 40% cytotoxicity of cells expressing said protein encoded by SEQ ID NO:1.

25. The method of claim 23 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment induces at least 60% cytotoxicity of cells expressing said protein encoded by SEQ ID NO:1.

26. The method of claim 18 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment is an IgG 1 .

27. The method of claim 18 , wherein the monoclonal anti-CS1 antibody or anti-CS1 antigen binding fragment has a low level of or lacks fucose.

28. The method of claim 18 , further comprising administering to the patient an immunosuppressive drug.

29. The method of claim 18 , further comprising administering to the patient an immunodulator.

30. The method of claim 29 , further comprising administering to the patient an immunosuppressive drug.

31. The method of claim 28 , wherein the conjugate compound is administered after the immunosuppressive drug.

32. The method of claim 28 , wherein the conjugate compound is administered in combination with the immunosuppressive drug.

33. The method of claim 29 , wherein the conjugate compound is administered after the immunomodulator.

34. The method of claim 29 , wherein the conjugate compound is administered in combination with the immunomodulator.

35. The method of claim 30 , wherein the conjugate compound is administered after the immunosuppressive drug and the immunomodulator.

36. The method of claim 30 , wherein the conjugate compound is administered in combination with the immunosuppressive drug and the immunomodulator.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2014
From: WILLIAMS, MARNA; TSO, J. YUN; LANDOLFI, NICHOLAS F.
To: PROTEIN DESIGN LABS, INC.
Reel/Frame 032174/0919 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2014
From: PDL BIOPHARMA, INC.
To: FACET BIOTECH CORPORATION
Reel/Frame 032175/0044 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2014
From: LIU, GAO
To: PDL BIOPHARMA
Reel/Frame 032175/0099 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 7, 2014
From: PDL BIOPHARMA, INC.
To: FACET BIOTECH CORPORATION
Reel/Frame 032175/0160 →
CHANGE OF NAME Recorded Feb 7, 2014
From: ABBOTT BIOTHERAPEUTICS CORP.
To: ABBVIE BIOTHERAPEUTICS INC.
Reel/Frame 032175/0225 →
CHANGE OF NAME Recorded Feb 7, 2014
From: PROTEIN DESIGN LABS, INC.
To: PDL BIOPHARMA, INC.
Reel/Frame 032188/0810 →
CHANGE OF NAME Recorded Feb 7, 2014
From: FACET BIOTECH CORPORATION
To: ABBOTT BIOTHERAPEUTICS CORP.
Reel/Frame 032188/0869 →