Antibodies against CD73 and uses thereof

Patent metadata

Field	Value
Publication number	US-10100129-B2
Application number	US-201515520638-A
Country	US
Kind code	B2
Filing date	Nov 19, 2015
Priority date	Nov 21, 2014
Publication date	Oct 16, 2018
Grant date	Oct 16, 2018

Abstract

The present disclosure provides isolated monoclonal antibodies, particularly human antibodies, that bind to human Cluster of Differentiation 73 (CD73) with high affinity, and inhibit the activity of CD73, and optionally mediate antibody dependent CD73 internalization. Nucleic acid molecules encoding the antibodies of the disclosure, expression vectors, host cells and methods for expressing the antibodies of the disclosure are also provided. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of the disclosure are also provided. The disclosure also provides methods for inhibiting the growth of a tumor cell expressing CD73 using the antibodies of the disclosure, including methods for treating various cancers.

First claim

We claim:

1. An isolated antibody, or antigen binding portion thereof, that binds to human Cluster of Differentiation 73 (CD73), and comprises a heavy chain comprising CDR1, CDR2, and CDR3 sequences comprising the amino acid sequences of SEQ ID NOs: 5, 6, and 7, respectively, and a light chain comprising CDR1, CDR2, and CDR3 sequences comprising the amino acid sequences of SEQ ID NOs: 13, 14, and 15, respectively.

2. The isolated antibody, or antigen binding portion thereof, of claim 1 , which binds to human CD73 with a K D of 0.1 nM to 10 nM, as determined by Surface Plasmon Resonance (SPR).

3. The isolated antibody, or antigen binding portion thereof, of claim 1 , which inhibits the activity of human CD73.

4. The isolated antibody, or antigen binding portion thereof, of claim 1 , which mediates internalization of human CD73.

5. The isolated antibody, or antigen binding portion thereof, of claim 1 , which has reduced effector function relative to a wild type IgG1 antibody.

6. The isolated antibody, or antigen binding portion thereof, of claim 1 , which is a human IgG antibody.

7. The isolated antibody, or antigen binding portion thereof, of claim 1 , which is a human IgG1, IgG2, or IgG4 antibody.

8. The isolated antibody, or antigen binding portion thereof, of claim 1 , comprising heavy and light chain variable regions, wherein the heavy and light chain variable regions comprise the amino acid sequences of SEQ ID NOs: 135 and 12, respectively.

9. The isolated antibody, or antigen binding portion thereof, of claim 1 , comprising heavy and light chain variable regions, wherein the heavy and light chain variable regions consist of the amino acid sequences of SEQ ID NOs: 135 and 12, respectively.

10. The isolated antibody, or antigen binding portion thereof, of claim 1 , comprising a heavy chain sequence comprising the amino acid sequence of SEQ ID NO: 133 or 189 and a light chain sequence comprising the amino acid sequence of SEQ ID NO: 102.

11. The isolated antibody, or antigen binding portion thereof, of claim 1 , comprising two heavy chains and two light chains, wherein each of the heavy chains consists of the amino acid sequence of SEQ ID NO: 133 or 189 and each of the light chains consists of the amino acid sequence of SEQ ID NO: 102.

12. The isolated antibody, or antigen binding portion thereof, of claim 11 , further comprising intermolecular disulfide bonding between the two heavy chain constant regions.

13. A composition comprising the antibody, or antigen binding portion thereof, of claim 1 , and a pharmaceutically acceptable carrier.

14. The composition of claim 13 , further comprising one or more additional therapeutic agents.

15. The composition of claim 14 , wherein the additional therapeutic agent is a programmed cell death protein 1 (PD-1) antagonist, a programmed death-ligand 1 (PD-L1)antagonist, a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antagonist, and/or a lymphocyte activation gene-3 (LAG-3) antagonist.

16. A composition comprising the antibody, or antigen binding portion thereof, of claim 8 , and a pharmaceutically acceptable carrier.

17. The composition of claim 16 , further comprising one or more additional therapeutic agents.

18. The composition of claim 17 , wherein the additional therapeutic agent is a programmed cell death protein 1 (PD-1) antagonist, a programmed death-ligand 1 (PD-L1) antagonist, a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antagonist, and/or a lymphocyte activation gene-3 (LAG-3) antagonist.

19. A composition comprising the antibody, or antigen binding portion thereof, of claim 9 , and a pharmaceutically acceptable carrier.

20. The composition of claim 19 , further comprising one or more additional therapeutic agents.

21. The composition of claim 20 , wherein the additional therapeutic agent is a programmed cell death protein 1 (PD-1) antagonist, a programmed death-ligand 1 (PD-L1) antagonist, a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antagonist, and/or a lymphocyte activation gene-3 (LAG-3) antagonist.

22. A composition comprising the antibody, or antigen binding portion thereof, of claim 10 , and a pharmaceutically acceptable carrier.

23. The composition of claim 22 , further comprising one or more additional therapeutic agents.

24. The composition of claim 23 , wherein the additional therapeutic agent is a programmed cell death protein 1 (PD-1) antagonist, a programmed death-ligand 1 (PD-L1) antagonist, a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antagonist, and/or a lymphocyte activation gene-3 (LAG-3) antagonist.

25. An isolated antibody, or antigen binding portion thereof, which comprises heavy and light chain variable regions, wherein the heavy and light chain variable regions comprise the amino acid sequences of SEQ ID NOs: 135 and 12, respectively.

26. The isolated antibody, or antigen binding portion thereof, of claim 25 , comprising heavy and light chain variable regions, wherein the heavy and light chain variable regions consist of the amino acid sequences of SEQ ID NOs: 135 and 12, respectively.

27. The isolated antibody, or antigen binding portion thereof, of claim 25 , comprising a heavy chain sequence comprising the amino acid sequence of SEQ ID NO: 133 or 189 and a light chain sequence comprising the amino acid sequence of SEQ ID NO: 102.

28. The isolated antibody, or antigen binding portion thereof, of claim 25 comprising two heavy chains and two light chains, wherein each of the heavy chains consists of the amino acid sequence of SEQ ID NO: 133 or 189 and each of the light chains consists of the amino acid sequence of SEQ ID NO: 102.

29. The isolated antibody, or antigen binding portion thereof, of claim 28 , further comprising intermolecular disulfide bonding between the two heavy chain constant regions.

30. A composition comprising the antibody, or antigen binding portion thereof, of claim 25 , and a pharmaceutically acceptable carrier.

31. The composition of claim 30 , further comprising one or more additional therapeutic agents.

32. The composition of claim 31 , wherein the additional therapeutic agent is a programmed cell death protein 1 (PD-1) antagonist, a programmed death-ligand 1 (PD-L1) antagonist, a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) antagonist, and/or a lymphocyte activation gene-3 (LAG-3) antagonist.

33. A composition comprising the antibody, or antigen binding portion thereof, of claim 27 , and a pharmaceutically acceptable carrier.

34. The composition of claim 33 , further comprising one or more additional therapeutic agents.

35. The composition of claim 34 , wherein the additional therapeutic agent is a PD-1 antagonist, a PD-L1 antagonist, CTLA-4 antagonist, and/or a LAG-3 antagonist.

Assignees

• Bristol Myers Squibb Co

Inventors

• Lonberg Nils
• Korman Alan J
• Barnhart Bryan C
• Yamniuk Aaron P
• Srinivasan Mohan
• Henning Karla A
• Lei Ming
• Sega Emanuela
• Goodenough Angela
• Jure-Kunkel Maria
• Chen Guodong
• Sack John S
• Huang Richard Y
• Corbett Martin J
• Myers Jr Joseph E
• Schweizer Liang
• Hatcher Sandra V
• Huang Haichun
• Zhang Pingping

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61P35/04

  specific for metastasis · CPC title

• A61P35/02

  specific for leukemia · CPC title

• G01N33/5759

  involving compounds localised on the membrane of tumour or cancer cells · CPC title

• C07K16/40 Primary

  against enzymes · CPC title