IP Library Granted Patent US 11,352,440
Granted Patent B2
US 11,352,440 · App. 16/117,183 · Granted Jun 7, 2022

Antibodies against CD73 and uses thereof

Inventors: Nils Lonberg (Woodside, CA); Alan J. Korman (Piedmont, CA); Bryan C. Barnhart (San Francisco, CA); Aaron P. Yamniuk (Lawrenceville, NJ); Mohan Srinivasan (Cupertino, CA); Karla A. Henning (Milpitas, CA); Ming Lei (Princeton, NJ); Emanuela Sega (Cupertino, CA); Angela Goodenough (Morrisville, PA); Maria N. Jure-Kunkel (Plainsboro, NJ); Guodong Chen (East Brunswick, NJ); John S. Sack (Lawrenceville, NJ); Richard Y. Huang (Bridgewater, NJ); Martin J. Corbett (Mount Holly, NJ); Joseph E. Myers, Jr. (Flemington, NJ); Liang Schweizer (Cambridge, MA); Sandra V. Hatcher (Hillsborough, NJ); Haichun Huang (Fremont, CA); Pingping Zhang (Cupertino, CA)
Assignee: BRISTOL-MYERS SQUIBB COMPANY
C07K16/40A61K39/3955A61K39/39558A61K45/06A61K47/6871C07K16/2896C07K16/30C07K16/303C07K16/3015C07K16/3023C07K16/3038C07K16/3046C07K16/3053C07K16/3061C07K16/3069G01N33/573G01N33/57492A61K2039/505C07K2317/21C07K2317/24C07K2317/31C07K2317/33C07K2317/34C07K2317/52C07K2317/522C07K2317/524C07K2317/526C07K2317/53C07K2317/54C07K2317/55C07K2317/56C07K2317/565C07K2317/567C07K2317/71C07K2317/72C07K2317/76C07K2317/77C07K2317/92C07K2317/94G01N2333/916
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Quick Facts
Patent No.
US 11,352,440
App. No.
16/117,183
Granted
Jun 7, 2022
Kind
B2
Abstract

The present invention 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 invention, expression vectors, host cells and methods for expressing the antibodies of the invention are also provided. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of the invention are also provided. The invention also provides methods for inhibiting the growth of a tumor cell expressing CD73 using the antibodies of the invention, including methods for treating various cancers.

Claims (18)

1. A method of decreasing adenosine levels in a tumor of a human subject, comprising administering to the subject an antibody that binds to human CD73, wherein the antibody 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. A method of stimulating an immune response against a tumor in a human subject in need thereof, comprising administering to the subject an effective amount of an antibody that binds to human CD73, wherein the antibody 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.

3. A method of stimulating an immune response in a human subject, comprising administering to the subject an antibody that binds to human CD73, wherein the antibody 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.

4. A method for inhibiting the growth of a tumor in a human subject comprising administering to the subject an antibody that binds to human CD73, wherein the antibody 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, and wherein the tumor is selected from the group consisting of breast, lung, colon, ovary, and prostate cancer tumors.

5. A method of treating cancer in a human subject, comprising administering to the subject a therapeutically effective amount of an antibody that binds to human CD73, wherein the antibody 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, and wherein the cancer is selected from the group consisting of breast, lung, colon, ovary, and prostate cancer.

6. The method of claim 5 , further comprising administering to the subject one or more additional therapeutic agents.

7. The method of claim 6 , wherein the additional therapeutic agent is a PD-1 antagonist, a PD-L1 antagonist, a CTLA-4 antagonist, or a LAG-3 antagonist.

8. The method of claim 5 , wherein the antibody comprises heavy and light chain variable regions comprising the amino acid sequences of SEQ ID NOs: 135 and 12, respectively.

9. The method of claim 8 , wherein the antibody comprises 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.

10. The method of claim 5 , wherein the heavy chain is a full-length heavy chain and the light chain is a full-length light chain.

11. The method of claim 8 , wherein the heavy chain is a full-length heavy chain and the light chain is a full-length light chain.

12. The method of claim 5 , wherein the antibody is an IgG antibody.

13. The method of claim 9 , wherein the antibody comprises a heavy chain consisting of the amino acid sequence of SEQ ID NO: 133 and a light chain consisting of the amino acid sequence of SEQ ID NO: 102.

14. The method of claim 9 , wherein the antibody comprises a heavy chain consisting of the amino acid sequence of SEQ ID NO: 189 and a light chain consisting of the amino acid sequence of SEQ ID NO: 102.

15. The method of claim 5 , wherein the antibody binds to human CD73 with a K D of 0.1 nM to 10 nM, as determined by Surface Plasmon Resonance (SPR).

16. The method of claim 5 , wherein the antibody inhibits the activity of human CD73.

17. The method of claim 5 , wherein the antibody mediates internalization of human CD73.

18. The method of claim 5 , wherein the antibody has reduced effector function relative to a wild type IgG1 antibody.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2020
From: LONBERG, NILS; KORMAN, ALAN J.; BARNHART, BRYAN C.; YAMNIUK, AARON P.; SRINIVASAN, MOHAN; HENNING, KARLA H.; LEI, MING; SEGA, EMANUELA; GOODENOUGH, ANGELA; JURE-KUNKEL, MARIA N.; CHEN, GUODONG; SACK, JOHN S.; HUANG, RICHARD; CORBETT, MARTIN J.; MYERS, JOSEPH E., JR.; SCHWEIZER, LIANG; HATCHER, SANDRA V.; HUANG, HAICHUN; ZHANG, PINGPING
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 051711/0113 →
Continuity (5)
Division 15432180 · Feb 14, 2017
Division 14994828 · Jan 13, 2016
Continuation PCTUS2015061639 · Nov 19, 2015
Provisional Application 62083056 · Nov 21, 2014
Related Publication 20190062456A1 · Feb 28, 2019