Binding molecules specific for CD73 and uses thereof

Patent metadata

Field	Value
Publication number	US-10287362-B2
Application number	US-201815903649-A
Country	US
Kind code	B2
Filing date	Feb 23, 2018
Priority date	Nov 10, 2014
Publication date	May 14, 2019
Grant date	May 14, 2019

Abstract

The present disclosure provides anti-CD73 binding molecules, e.g., antibodies and antigen binding fragments thereof. Also provided are pharmaceutical formulations comprising the disclosed compositions, and methods for the diagnosis and treatment of diseases associated with CD73-expression, e.g., cancer. Such diseases can be treated, e.g., by direct therapy with the anti-CD73 binding molecules disclosed herein (e.g., naked antibodies or antibody-drug conjugates that bind CD73), by adjuvant therapy with other antigen-binding anticancer agents such as immune checkpoint inhibitors (e.g., anti-CTLA-4 and anti-PD-1 monoclonal antibodies), and/or by combination therapies where the anti-CD73 molecules are administered before, after, or concurrently with chemotherapy.

First claim

What is claimed is:

1. A method of treating a CD73-associated cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of an antibody or antigen-binding fragment thereof that specifically binds to CD73, wherein the antibody or antigen-binding fragment thereof comprises a heavy chain VH domain and a light chain VL domain, the heavy and light chain domains comprising:
(a) a VH CDR1 having the amino acid sequence of SEQ ID NO: 36;
(b) a VH CDR2 having the amino acid sequence of SEQ ID NO: 39;
(c) a VH CDR3 having the amino acid sequence of SEQ ID NO: 45;
(d) a VL CDR1 having the amino acid sequence of SEQ ID NO: 46;
(e) a VL CDR2 having the amino acid sequence of SEQ ID NO: 51; and
(f) a VL CDR3 having the amino acid sequence of SEQ ID NO: 56.

2. The method of claim 1 , wherein the antibody VL domain comprises the amino acid sequence of SEQ ID NO: 68; and wherein the antibody VH domain comprises the amino acid sequence of SEQ ID NO: 82.

3. The method according to claim 1 , wherein the cancer is selected from the group consisting of colorectal cancer, pancreatic cancer, bladder cancer, leukemia, lymphoma, glioma, glioblastoma, melanoma, ovarian cancer, thyroid cancer, esophageal cancer, prostate cancer, and breast cancer.

4. A method of treating a CD73-associated cancer in a subject comprising administering to the subject a therapeutically effective amount of a first agent which is the antibody or antigen-binding fragment thereof according to either one of claim 1 or 2 , in combination with a therapeutically effective amount of a second agent, which is an anti-cancer agent other than the first agent.

5. The method according to claim 4 , wherein the combination of the first agent and the second agent is additively or synergistically effective.

6. The method according to claim 4 , wherein the second agent specifically binds to PD-1 (programmed death 1 protein), PD-L1 (programmed death 1 protein ligand 1), PD-L2 (programmed death 1 protein ligand 2), or CTLA-4 (cytotoxic T lymphocyte antigen 4 protein).

7. The method according to claim 4 , where the second agent comprises an anti-CTLA- 4 antibody or antigen binding fragment thereof.

8. The method according to claim 7 , wherein the anti-CTLA-4 antibody is tremelimumab (ticilimumab, CP-675,206).

9. The method according to claim 4 , wherein the second agent comprises an anti-PD-L1 antibody or antigen-binding fragment thereof.

10. The method of claim 9 , therein the anti-PD-L1antibody is MEDI4736.

11. A method of treatment comprising administering an anti-CD73 antibody, or an antigen binding fragment thereof, to a subject identified as having a tumor that has increased expression of CD73 relative to a reference, and wherein the anti-CD73 antibody is MEDI9447.

12. The method of claim 11 , wherein the subject is undergoing, has undergone, or will undergo an anti-PD-1, anti-PD-L1, or anti-CTLA4 therapy.

13. The method of claim 12 , wherein the anti-PD-1, anti-PD-L1, or anti-CTLA4 therapy comprises administering an anti-PD-1, anti-PD-L1, or anti-CTLA4 antibody or antigen binding fragment thereof.

14. The method of claim 13 , wherein the anti-PD-L1 antibody is MEDI4736, BMS-936559, or MPDL3280A or antigen-binding fragments thereof.

15. The method of claim 13 , wherein the anti-CTLA-4 antibody is ipilimumab, tremelimumab (ticilimumab, CP-675,206), or an antigen binding fragment thereof.

Assignees

• Medimmune Ltd

Inventors

• Hay Carl
• Sachsenmeier Kris
• Sult Erin
• Huang Qihui
• Pavlik Peter
• Damschroder Melissa
• Cheng Li
• Diedrich Gundo
• Rios-Doria Jonathan
• Hammond Scott
• Minter Ralph
• Rust Steve
• Guillard Sandrine
• Hollingsworth Robert
• Jermutus Lutz
• Durham Nicholas
• Leow Ching Ching
• Antonysamy Mary
• Geoghegan James
• Lu Xiaojun
• Rosenthal Kim

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61P35/02

  specific for leukemia · CPC title

• A61K39/3955 Primary

  against proteinaceous materials, e.g. enzymes, hormones, lymphokines · CPC title

• C07K2317/77

  Internalization into the cell · CPC title

• C07K2317/30

  characterized by aspects of specificity or valency · CPC title