IP Library Granted Patent US 9,988,450
Granted Patent B2
US 9,988,450 · App. 15/802,093 · Granted Jun 5, 2018

Anti-PD1 antibodies and their use as therapeutics and diagnostics

Inventors: Kang Li (Beijing, CN); Tong Zhang (Beijing, CN); Jing Song (Beijing, CN); Lanlan Xu (Beijing, CN); Qi Liu (Beijing, CN); Hao Peng (Beijing, CN)
Assignee: BEIGENE SWITZERLAND GMBH
C07K16/2803A61K39/39591C07K16/2818A61K2039/505C07K2317/24C07K2317/33C07K2317/34C07K2317/52C07K2317/53C07K2317/55C07K2317/565C07K2317/567C07K2317/70C07K2317/71C07K2317/73C07K2317/76C07K2317/92C07K2317/94
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,988,450
App. No.
15/802,093
Granted
Jun 5, 2018
Kind
B2
Abstract

Provided are antibodies that specifically bind to Programmed Death-1 (PD1, Pdcd-1, or CD279) and inhibit PD1-mediated cellular signaling and activities in immune cells, antibodies binding to a set of amino acid residues required for its ligand binding, and uses of these antibodies to treat or diagnose cancer, infectious diseases or other pathological disorders modulated by PD1-mediated functions.

Claims (29)

1. A method of treating cancer in a subject in need thereof, the method comprising administering to the subject a monoclonal antibody which binds human PD-1,

wherein the IgG Fc region of the antibody is an IgG4 Fc region containing an amino acid mutation at position 228 and at least one additional amino acid mutation,

wherein the at least one additional mutation causes the antibody to exhibit reduced binding to at least one Fcγ receptor relative to Fc binding of a reference IgG4 antibody having a mutation at position 228 and no other Fc region mutation, and

wherein the numbering of the residues in the IgG4 Fc region is that of the EU numbering system.

2. The method of claim 1 , wherein the position of the at least one additional amino acid mutation is selected from the group consisting of positions 233, 234, 235, 265, 309, and 409.

3. The method of claim 1 , wherein the IgG Fc region of the antibody contains at least two amino acid mutations in addition to the mutation at position 228.

4. The method of claim 1 , wherein the at least one additional amino acid mutation comprises mutations at positions 233, 234, and 235.

5. The method of claim 1 , wherein the at least one additional amino acid mutation comprises mutations at positions 233, 234, 235, and 265.

6. The method of claim 1 , wherein the at least one additional amino acid mutation comprises mutations at positions 233, 234, 235, 265, 309, and 409.

7. The method of claim 1 , wherein the at least one additional amino acid mutation comprises E233P, F234V, and L235A.

8. The method of claim 1 , wherein the amino acid mutation at position 228 is S228P, and the at least one additional amino acid mutation comprises E233P, F234V, and L235A.

9. The method of claim 1 , wherein the binding of the IgG4 Fc region of the antibody to one or more Fcγ receptors is reduced to null.

10. The method of claim 1 , wherein the at least one Fcγ receptor is selected from FcγRI, FcγRIIA, FcγRIIB, and FcγRIIIA.

11. The method of claim 1 , wherein the antibody exhibits reduced effector function relative to the reference IgG4 antibody.

12. The method of claim 6 , wherein the reduced effector function is antibody-dependent cell-mediated cytotoxicity (ADCC).

13. The method of claim 1 , wherein the mutation at position 228 is S228P.

14. The method of claim 1 , wherein the at least one additional amino acid mutation is selected from the group consisting of E233P, F234V, L235A, D265A, L309V, and R409K, or a combination thereof.

15. The method of claim 1 , wherein the cancer is selected from lung cancer, liver cancer, stomach cancer, breast cancer, ovarian cancer, pancreatic cancer, esophageal cancer, and melanoma.

16. The method of claim 1 , wherein the antibody exhibits anti-tumor activity.

17. The method of claim 1 , wherein the administration of the antibody inhibits tumor progression in the subject.

18. The method of claim 1 , wherein the administration of the antibody suppresses PD-1 mediated signal transduction.

19. A monoclonal antibody which binds human PD-1, comprising,

a PD-1 binding domain, and

an IgG4 Fc region comprising amino acid mutations at positions 228, 233, 234, and 235,

wherein the mutations at positions 233, 234, and 235 cause the antibody to exhibit reduced binding to at least one Fcγ receptor relative to Fc binding of a reference IgG4 antibody having a mutation at position 228 and no other Fc region mutation, and

wherein the numbering of the residues in the IgG4 Fc region is that of the EU numbering system.

20. The antibody of claim 19 , wherein the IgG4 Fc region comprising amino acid mutations at positions 228, 233, 234, 235, and 265.

21. The antibody of claim 19 , wherein the IgG4 Fc region comprising amino acid mutations at positions 228, 233, 234, 235, 265, 309, and 409.

22. The antibody of claim 19 , wherein the IgG4 Fc region comprising amino acid mutations of S228P, E233P, F234V, and L235A.

Assignments (4)
CHANGE OF NAME Recorded Sep 23, 2025
From: BEIGENE SWITZERLAND GMBH
To: BEONE MEDICINES I GMBH
Reel/Frame 072872/0076 →
CHANGE OF ASSIGNEE ADDRESS Recorded Nov 4, 2021
From: BEIGENE SWITZERLAND GMBH
To: BEIGENE SWITZERLAND GMBH
Reel/Frame 058267/0358 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 11, 2017
From: BEIGENE, LTD.
To: BEIGENE SWITZERLAND GMBH
Reel/Frame 044353/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2017
From: LI, KANG; ZHANG, TONG; SONG, JING; XU, LANLAN; LIU, QI; PENG, HAO
To: BEIGENE, LTD.
Reel/Frame 044022/0481 →
Continuity (6)
Continuation 14736966 · Jun 11, 2015
Continuation PCTCN2013083467 · Sep 13, 2013
Division 14194797 · Mar 2, 2014
Division 14076214 · Nov 10, 2013
Continuation PCTCN2013083467 · Sep 13, 2013
Related Publication 20180111995A1 · Apr 26, 2018