IP Library Granted Patent US 11,214,619
Granted Patent B2
US 11,214,619 · App. 17/261,463 · Granted Jan 4, 2022

Anti-CD112R compositions and methods

Inventors: Bianka Prinz (Lebanon, NH); Nadthakarn Boland (Lebanon, NH); Kevin Schutz (Lebanon, NH); John Bukowski (Lebanon, NH); Jennifer Symonds (Lebanon, NH); James Mohan (Cambridge, MA); Marisella Panduro Sicheva (Cambridge, MA)
Assignee: SURFACE ONCOLOGY, INC.
C07K16/2818A61P35/00A61P37/04C07K16/2803C07K16/2827A61K45/06A61K2039/505A61K2039/507C07K2317/52C07K2317/73C07K2317/74C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 11,214,619
App. No.
17/261,463
Granted
Jan 4, 2022
Kind
B2
Abstract

The invention provides anti-CD112R antibody compositions and their use in treating cancer.

Claims (28)

1. An isolated antibody or antigen binding portion thereof, that binds to CD112R and comprises:

a. a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 701;

b. a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 702;

c. a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 703;

d. a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 704;

e. a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 705; and

f. a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 706.

2. The isolated antibody or antigen binding portion thereof, of claim 1 , wherein the isolated antibody or antigen binding portion thereof comprises a heavy chain variable region having a sequence at least 90% identical to the amino acid sequence of SEQ ID NO: 712 and a light chain variable region having a sequence at least 90% identical to the amino acid sequence of SEQ ID NO: 718.

3. The isolated antibody or antigen binding portion thereof, of claim 2 , wherein the isolated antibody or antigen binding portion thereof comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 712 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 718.

4. The isolated antibody or antigen binding portion thereof, of claim 3 , wherein the isolated antibody is a monoclonal antibody.

5. The isolated antibody or antigen binding portion thereof, of claim 3 , wherein the isolated antibody is fully human or humanized.

6. The isolated antibody or antigen binding portion thereof, of claim 3 , wherein an Fc region of the isolated antibody comprises IgG1, IgG2, IgG3, or IgG4.

7. The isolated antibody or antigen binding portion thereof, of claim 6 , wherein the isolated antibody comprises a human IgG1 heavy chain constant region.

8. The isolated antibody or antigen binding portion thereof, of claim 6 , wherein the isolated antibody comprises a human IgG4 heavy chain constant region.

9. The isolated antibody or antigen binding portion thereof, of claim 8 , wherein the isolated antibody comprises a mutant human IgG4 heavy chain constant region.

10. The isolated antibody or antigen binding portion thereof, of claim 9 , wherein the mutant IgG4 heavy chain constant region comprises a mutation selected from a substitution at Ser228, a substitution at Leu235, a substitution at Asn297, or a combination thereof, numbering according to EU numbering.

11. The isolated antibody or antigen binding portion thereof, of claim 10 , wherein the mutant IgG4 heavy chain constant region comprises an S228P substitution and an L235E substitution, numbering according to EU numbering.

12. The isolated antibody or antigen binding portion thereof, of claim 1 , wherein the CD112R is a human CD112R.

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

14. The pharmaceutical composition of claim 13 , further comprising at least one additional therapeutic agent.

15. The pharmaceutical composition of claim 13 , further comprising:

a. an antagonist of PD-1, PD-L1, CTLA-4, Lag-3, TIM-3, TIGIT, CD96, PVRL1, PVRL2, PVRL3, PVRL4, CD155, CD47, CD39 or IL-27;

b. a STING agonist; or

c. a combination of (a) and (b).

16. The pharmaceutical composition of claim 13 , further comprising an antagonist of TIGIT.

17. The pharmaceutical composition of claim 13 , further comprising an antagonist of CD96.

18. The pharmaceutical composition of claim 13 , further comprising an antagonist of PD-1 or PD-L1.

19. The pharmaceutical composition of claim 13 , further comprising two or more of an antagonist of PD-1, an antagonist PD-L1, an antagonist of TIGIT, and/or an antagonist of CD96.

Assignments (4)
SECURITY INTEREST Recorded May 8, 2024
From: COHERUS BIOSCIENCES, INC.; COHERUS INTERMEDIATE CORP.; INTEKRIN THERAPEUTICS INC.; SURFACE ONCOLOGY, LLC; COHERUS ONCOLOGY SUPPORTIVE CARE LLC
To: ANKURA TRUST COMPANY, LLC
Reel/Frame 067348/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2021
From: MOHAN, JAMES; SICHEVA, MARISELLA PANDURO
To: SURFACE ONCOLOGY, INC.
Reel/Frame 057751/0333 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2021
From: PRINZ, BIANKA; BOLAND, NADTHAKARN; SCHUTZ, KEVIN; BUKOWSKI, JOHN; SYMONDS, JENNIFER
To: ADIMAB, LLC
Reel/Frame 057751/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 11, 2021
From: ADIMAB, LLC
To: SURFACE ONCOLOGY, INC.
Reel/Frame 057751/0979 →
Continuity (3)
Provisional Application 62844958 · May 8, 2019
Provisional Application 62701065 · Jul 20, 2018
Related Publication 20210253699A1 · Aug 19, 2021
Cited By (1)
US 12,269,888