IP Library Granted Patent US 12,281,163
Granted Patent B2
US 12,281,163 · App. 17/038,863 · Granted Apr 22, 2025

Dimers and use thereof

Inventors: Ting Xu (Suzhou, CN); Kangping Guo (Suzhou, CN); Dong Yang (Suzhou, CN); Pilin Wang (Suzhou, CN); Yuhao Jin (Suzhou, CN); Xiaoxiao Wang (Suzhou, CN)
Assignee: JIANGSU ALPHAMAB BIOPHARMACEUTICALS CO., LTD.
C07K16/2818C07K16/2827A61K2039/505C07K2317/52
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Quick Facts
Patent No.
US 12,281,163
App. No.
17/038,863
Granted
Apr 22, 2025
Kind
B2
Abstract

The present disclosure provides a dimer formed by two polypeptide chains, with each of the two polypeptide chains comprising an antibody Fc subunit, wherein the dimer comprises two or more immunoglobulin single variable domains (ISVDs), at least one of the ISVDs is specific for PD-L1, and at least one of the ISVDs is specific for CTLA4.

Claims (18)

1. A dimer formed by two polypeptide chains, with each of said two polypeptide chains comprising an antibody Fc subunit, wherein said dimer comprises two or more immunoglobulin single variable domains (ISVDs), at least one of said ISVDs is specific for PD-L1, and at least one of said ISVDs is specific for CTLA4;

wherein said ISVD specific for PD-L1 comprises a heavy chain CDR1, CDR2, and CDR3 comprising the amino acid sequences set forth in SEQ ID NOs: 3, 4, and 5, respectively;

wherein said ISVD specific for CTLA4 comprises a heavy chain CDR1, CDR2, and CDR3 comprising the amino acid sequences set forth in SEQ ID NOs: 17, 18, and 19, respectively;

wherein the C-terminus of said ISVD specific for PD-L1 is fused to the N-terminus of the antibody Fc subunit via a linker; and

wherein said dimer is a homodimer.

2. The dimer according to claim 1 , wherein said antibody Fc subunit is derived from an IgG Fc subunit.

3. The dimer according to claim 1 , wherein said antibody Fc subunit comprises an amino acid sequence as set forth in any one of SEQ ID NOs: 35, 38 and 39.

4. The dimer according to claim 1 , wherein said ISVD specific for PD-L1 is capable of binding to the N-terminal IgV domain of human PD-L1.

5. The dimer according to claim 1 , wherein said ISVD specific for PD-L1 comprises a heavy chain variable domain comprising an amino acid sequence as set forth in any one of SEQ ID NOs: 6, 13, 14 and 15.

6. The dimer according to claim 1 , wherein said ISVD specific for CTLA4 comprises a heavy chain variable domain comprising an amino acid sequence as set forth in any one of SEQ ID NOs: 20 and 30-32.

7. The dimer according to claim 1 , wherein one or both of said two polypeptide chains comprises an amino acid sequence as set forth in SEQ ID NO: 42 or 43.

8. The dimer according to claim 1 , which is capable of blocking binding of PD-L1 to PD-1.

9. The dimer according to claim 1 , which is capable of blocking binding of PD-L1 to CD80.

10. The dimer according to claim 1 , which is capable of blocking binding of CTLA4 to CD80.

11. The dimer according to claim 1 , which is capable of blocking binding of CTLA4 to CD86.

12. An immunoconjugate, comprising the dimer according to claim 1 .

13. A pharmaceutical composition comprising an effective amount of the dimer according to claim 1 and a pharmaceutically acceptable excipient.

14. A method for treating a cancer in a subject in need thereof, comprising administering to said subject an effective amount of the dimer according to claim 1 .

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2021
From: XU, TING; GUO, KANGPING; YANG, DONG; WANG, PILIN; JIN, YUHAO
To: JIANGSU ALPHAMAB BIOPHARMACEUTICALS CO., LTD.
Reel/Frame 055182/0369 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2021
From: WANG, XIAOXIAO
To: JIANGSU ALPHAMAB BIOPHARMACEUTICALS CO., LTD.
Reel/Frame 055182/0557 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 23, 2020
From: SUZHOU ALPHAMAB CO., LTD.
To: JIANGSU ALPHAMAB BIOPHARMACEUTICALS CO., LTD.
Reel/Frame 054149/0786 →
Priority Claims (2)
WO PCT/CN2018/090012 · Jun 5, 2018 · international
WO PCT/CN2019/086821 · May 14, 2019 · international
Continuity (2)
Continuation PCTCN2019089980 · Jun 4, 2019
Related Publication 20210095031A1 · Apr 1, 2021
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