Bispecific antibodies

Patent metadata

Field	Value
Publication number	US-2016145355-A1
Application number	US-201414900757-A
Country	US
Kind code	A1
Filing date	Jun 20, 2014
Priority date	Jun 24, 2013
Publication date	May 26, 2016
Grant date	—

Abstract

The present invention provides, inter alia, bispecific antibodies containing a first antigen binding moiety that specifically binds an epitope on human cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and a second antigen binding moiety that specifically binds an epitope on a human programmed death 1 (PD-1) receptor. Also provided are pharmaceutical compositions containing such bispecific antibodies, as well as methods and kits for treating cancer using such bispecific antibodies and pharmaceutical compositions.

First claim

What is claimed is:

1 . A bispecific antibody comprising:
(a) a first antigen binding moiety that specifically binds an epitope on human cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), the first antigen binding moiety comprising an antibody having:
(1) a heavy chain CDR1 comprising SYTMH (SEQ ID NO:21), a heavy chain CDR2 comprising FISYDGNNKYYADSVKG (SEQ ID NO:22), and a heavy chain CDR3 comprising TGWLGPFDY (SEQ ID NO:23); and
(2) a light chain CDR1 comprising RASQSVGSSYLA (SEQ ID NO:18), a light chain CDR2 comprising GAFSRAT (SEQ ID NO:19), and a light chain CDR3 comprising QQYGSSPWT (SEQ ID NO:20); and
(b) a second antigen binding moiety that specifically binds an epitope on a human programmed death 1 (PD-1) receptor, the second antigen binding moiety comprising an antibody having:
(1) a heavy chain CDR1 comprising NSGMH (SEQ ID NO:27), a heavy chain CDR2 comprising VIWYDGSKRYYADSVKG (SEQ ID NO:28), and a heavy chain CDR3 comprising NDDYW (SEQ ID NO:29); and
(2) a light chain CDR1 comprising RASQSVSSYL (SEQ ID NO:24), a light chain CDR2 comprising DASNRAT (SEQ ID NO:25), and a light chain CDR3 comprising QQSSNWPRT (SEQ ID NO:26).

2 . The bispecific antibody of claim 1 , wherein the first antigen binding moiety specifically binds an epitope in the extracellular IgV domain of the human CTLA-4.

3 . The bispecific antibody of claim 1 , wherein the second antigen binding moiety specifically binds an epitope in the extracellular IgV domain of the human PD-1 receptor.

4 . The bispecific antibody of claim 1 , which is a recombinant antibody, a monoclonal antibody, a chimeric antibody, a humanized antibody, a human antibody, or an antibody fragment.

5 . The bispecific antibody of claim 1 in which the first antigen binding moiety comprises a variable heavy chain as depicted in SEQ ID NO:5, a variable light chain as depicted in SEQ ID NO:6 and the second antigen binding moiety comprises a variable heavy chain as depicted in SEQ ID NO:11, a variable light chain as depicted in SEQ ID NO:12.

6 . The bispecific antibody of claim 1 , wherein the first and second first antigen binding moieties are connected directly or by a linker.

7 . The bispecific antibody of claim 6 , wherein the linker is selected from the group consisting of a chemical linker or a polypeptide linker.

8 . The bispecific antibody of claim 1 , wherein the bispecific antibody is bivalent, trivalent, or tetravalent.

9 . A bispecific antibody comprising:
(a) a first antigen binding moiety that specifically binds an epitope on human cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), and (b) a second antigen binding moiety that specifically binds an epitope on a human programmed death 1 (PD-1) receptor.

10 . The bispecific antibody of claim 9 , wherein the first antigen binding moiety specifically binds an epitope in the extracellular IgV domain of the human CTLA-4.

11 . The bispecific antibody of claim 9 , wherein the second antigen binding moiety specifically binds an epitope in the extracellular IgV domain of the human PD-1 receptor.

12 . The bispecific antibody of claim 9 , which is a recombinant antibody, a monoclonal antibody, a chimeric antibody, a humanized antibody, a human antibody, or an antibody fragment.

13 . The bispecific antibody of claim 9 , wherein the first and second antigen binding moieties are connected directly or by a linker.

14 . The bispecific antibody of claim 13 , wherein the linker is selected from the group consisting of a chemical linker or a polypeptide linker.

15 . The bispecific antibody of claim 9 , wherein the first antigen binding moiety comprises a variable heavy chain and a variable light chain of ipilimumab, and the second antigen binding moiety comprises a variable heavy chain and a variable light chain of nivolumab.

16 . The bispecific antibody of claim 9 , wherein the first antigen binding moiety comprises a variable heavy chain and a variable light chain of tremelimumab, and the second antigen binding moiety comprises a variable heavy chain and a variable light chain of nivolumab.

17 . The bispecific antibody of claim 9 , wherein each antigen binding moiety is independently selected from the group consisting of IgM, IgG, IgD, IgA, IgE, antibody fragments that retain antigen recognition and binding capability that are Fab, Fab′, F(ab′) 2 , and Fv fragments, and combinations thereof, and further wherein the first and second antigen binding moieties are connected directly or by a linker.

18 . The bispecific antibody of claim 9 , wherein the bispecific antibody is bivalent, trivalent, or tetravalent.

19 . The bispecific antibody of claim 9 , wherein the bispecific antibody is selected from the group consisting of a tandem scFv (taFv or scFv 2 ), diabody, dAb 2 /VHH 2 , knob-into-holes derivates, SEED-IgG, heteroFc-scFv, Fab-scFv, scFv-Jun/Fos, Fab′-Jun/Fos, tribody, DNL-F(ab) 3 , scFv 3 -CH1/CL, Fab-scFv 2 , IgG-scFab, IgG-scFv, scFv-IgG, scFv 2 -Fc, F(ab′) 2 -scFv 2 , scDB-Fc, scDb-CH3, Db-Fc, scFv 2 -H/L, DVD-Ig, tandAb, scFv-dhlx-scFv, dAb 2 -IgG, dAb-IgG, dAb-Fc-dAb, and combinations thereof.

20 . The bispecific antibody of claim 9 , wherein the bispecific antibody is a diabody or a tribody.

21 . A pharmaceutical composition comprising a bispecific antibody of claim 1 and a pharmaceutically acceptable excipient.

22 . A pharmaceutical composition comprising a bispecific antibody of claim 5 and a pharmaceutically acceptable excipient.

23 . A pharmaceutical composition comprising a bispecific antibody of claim 9 and a pharmaceutically acceptable excipient.

24 . A method of treating cancer in a subject, comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 21 .

25 . The method according to claim 24 , wherein the cancer is selected from the group consisting of melanoma, lung cancer, and renal cancer.

26 . The method according to claim 25 , wherein the cancer is melanoma.

27 . The method according to claim 25 , wherein the subject is human.

28 . A method of treating cancer in a subject comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 22 .

29 . The method according to claim 28 , wherein the cancer is selected from the group consisting of melanoma, lung cancer, and renal cancer.

30 . The method according to claim 29 , wherein the cancer is melanoma.

31 . The method according to claim 29 , wherein the subject is human.

32 . A method of treating cancer in a subject comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 23 .

33 . The method according to claim 32 , wherein the cancer is selected from the group consisting of melanoma, lung cancer, and renal cancer.

34 . The method according to claim 33 , wherein the cancer is melanoma.

35 . The method according to claim 33 , wherein the subject is human.

36 . A method of treating cancer in a subject comprising administering to the subject a therapeutically effective amount of a bispecific antibody one antigen binding moiety of which specifically binds human CTLA-4 and the other antigen bi

Assignees

• Biomed Valley Discoveries Inc

Inventors

• Saha Saurabh
• Roix Jeffrey James
• Welsch Dean

Classifications

• C07K16/2818 Primary

  against CD28 or CD152 · CPC title

• C07K2317/626

  Diabody or triabody · CPC title

• C07K16/2803

  against the immunoglobulin superfamily · CPC title

• C07K2317/565

  Complementarity determining region [CDR] · CPC title

• C07K16/468 Primary

  Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies · CPC title