IP Library › Granted Patent US 12,195,538
Granted Patent B2
US 12,195,538 · App. 17/298,741 · Granted Jan 14, 2025

Anti-PD-L1/anti-4-1BB bispecific antibodies and uses thereof

Inventors: Eunyoung Park (Seongnam-si, KR); Yangsoon Lee (Seongnam-si, KR); Hyejin Chung (Seongnam-si, KR); Eunsil Sung (Seongnam-si, KR); Jiseon Yoo (Seongnam-si, KR); Minji Park (Seongnam-si, KR); Yong-Gyu Son (Seongnam-si, KR); Hyoju Choi (Seongnam-si, KR); Eunjung Kim (Seongnam-si, KR); Jaeho Jung (Seongnam-si, KR); Weon-Kyoo You (Seongnam-si, KR); Sang Hoon Lee (Seongnam-si, KR); Lei Fang (Shanghai, CN); Wenqing Jiang (Shanghai, CN)
Assignees: ABL BIO INC.; I-MAB BIOPHARMA US LIMITED
C07K16/2827A61P35/00C07K16/2878C07K16/468C07K2317/21C07K2317/24C07K2317/31C07K2317/34C07K2317/565C07K2317/622C07K2317/64C07K2317/75C07K2317/92
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 12,195,538
App. No.
17/298,741
Granted
Jan 14, 2025
Kind
B2
Abstract

The present disclosure provides an anti-PD-L1/anti-4-1BB bispecific antibody capable to effectively block the interactions between PD-L1 and its receptor PD-1 and between 4-1BB and its ligand. The bispecific antibody may have high binding affinity to both of a PD-L1 protein and a 4-1BB protein.

Claims (12)

1. An anti-PD-L1/anti-4-1BB bispecific antibody, comprising an anti-PD-L1 antibody or an antigen-binding fragment thereof and an anti-4-1BB antibody or an antigen-binding fragment thereof, wherein

the anti-PD-L1 antibody or antigen-binding fragment thereof comprises a VH CDR1 comprising the amino acid sequence of SEQ ID NO: 1; a VH CDR2 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 2 and 3; a VH CDR3 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 4, 5, 262, 263, 264, 265, 266 and 267; a VL CDR1 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 6, 268 and 269; a VL CDR2 comprising the amino acid sequence of SEQ ID NO: 7; and a VL CDR3 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 8, 270, 271 and 272; and

the anti-4-1BB antibody or antigen-binding fragment thereof comprises a VH CDR1 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 10 and 11; a VH CDR2 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 12 and 13; a VH CDR3 comprising the amino acid sequence selected from the group consisting of SEQ ID NOS: 14, 15, 16 and 17; a VL CDR1 comprising the amino acid sequence of SEQ ID NO: 18; a VL CDR2 comprising the amino acid sequence of SEQ ID NO: 19; and a VL CDR3 comprising the amino acid sequence of SEQ ID NO: 20.

2. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , wherein the anti-PD-L1 antibody or antigen-binding fragment thereof is capable of specifically binding to an immunoglobulin C (Ig C) domain of a human Programmed death-ligand 1 (PD-L1) protein, wherein the Ig C domain consists of amino acid residues 133-225.

3. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , wherein the anti-PD-L1 antibody or antigen-binding fragment thereof does not bind to an immunoglobulin V (Ig V) domain of the PD-L1 protein, wherein the Ig V domain consists of amino acid residues 19-127.

4. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , wherein the anti-PD-L1 antibody or antigen-binding fragment thereof comprises a heavy chain variable region comprising an amino acid sequence selected from the group consisting of SEQ ID NOS: 103, and 104, or a polypeptide having at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOS: 103, and 104.

5. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , wherein the anti-PD-L1 antibody or antigen-binding fragment thereof comprises a light chain variable region comprising an amino acid sequence selected from the group consisting of SEQ ID NOS: 105, and 106, or a peptide having at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOS: 105, and 106.

6. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , wherein the anti-4-1BB antibody or antigen-binding fragment thereof comprises a heavy chain variable region comprising an amino acid sequence selected from the group consisting of SEQ ID NOS: 21, 22, 23, and 24, or a polypeptide having at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOS: 21, 22, 23, and 24.

7. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , wherein the anti-4-1BB antibody or antigen-binding fragment thereof comprises a light chain variable region comprising an amino acid sequence selected from the group consisting of SEQ ID NOS: 25 and 26, or a peptide having at least 90% sequence identity to an amino acid sequence selected from the group consisting of SEQ ID NOS: 25 and 26.

8. The anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 , which is in the form of IgG-scFv form.

9. A method for treating a disease associated with PD-L1, 4-1BB, or both thereof, comprising administering to the patient a composition comprising the anti-PD-L1/anti-4-1BB bispecific antibody of claim 1 and a pharmaceutically acceptable carrier.

10. The method of claim 9 , wherein the disease associated with PD-L1, 4-1BB, or both thereof is cancer.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2024
From: I-MAB BIOPHARMA CO., LTD.
To: I-MAB BIOPHARMA US LIMITED
Reel/Frame 069267/0830 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2021
From: PARK, EUNYOUNG; LEE, YANGSOON; CHUNG, HYEJIN; SUNG, EUNSIL; YOO, JISEON; PARK, MINJI; SON, YONG-GYU; CHOI, HYOJU; KIM, EUNJUNG; JUNG, JAEHO; YOU, WEON-KYOO; LEE, SANG HOON; FANG, LEI; JIANG, WENQING
To: ABL BIO INC.; I-MAB BIOPHARMA CO., LTD.
Reel/Frame 056788/0312 →
Continuity (2)
Provisional Application 62773239 · Nov 30, 2018
Related Publication 20220056136A1 · Feb 24, 2022
References Cited (14)
US 20140302039A1 · Jeong · 2014 [cited by examiner]
US 20170198050A1 · Eckelman et al. · 2017 [cited by applicant]
CN 107326014A · 2017 [cited by applicant]
WO 2016061142A1 · 2016 [cited by applicant]
WO 2017215590A1 · 2017 [cited by applicant]
WO 2017220988A1 · 2017 [cited by applicant]
WO 2018045110A1 · 2018 [cited by applicant]
Chang-ling Gu, et al., “Bispecific antibody simultaneously targeting PD1 and HER2 inhibits tumor growth via direct tumor cell killing in combination with PD1/PDL1 blockade and HER2 inhibition”, Acta Pharmacologica Sinic… [cited by applicant]
Communication dated Sep. 20, 2023 in European Application No. 19 890 398.1. [cited by applicant]
Elisabeth Pérez-Ruiz, et al., “Anti-CD137 and PD-1/PD-L1 Antibodies En Route toward Clinical Synergy”, Clinical Cancer Research, Aug. 8, 2017, pp. 5326-5328, vol. 23, No. 18. [cited by applicant]
Shu-Juan Zhou, et al., “Strategies for Bispecific Single Chain Antibody in Cancer Immunotherapy”, Journal of Cancer, Oct. 17, 2017, pp. 3689-3696, vol. 8. [cited by applicant]
International Search Report for PCT/CN2019/075180 dated Aug. 27, 2019 [PCT/ISA/210]. [cited by applicant]
Written Opinion for PCT/CN2019/075180 dated Aug. 27, 2019 [PCT/ISA/237]. [cited by applicant]
Alexey Berezhnoy et al., “Converting PD-L1-induced T-lymphocyte Inhibition into CD137-mediated Costimulation via PD-L1 x CD137 Bispecific DART Molecules”, MacroGenics, 2018, Presented at the 30th EORTC/AACR/NCI Symposiu… [cited by applicant]
Cited By (1)
US 12,577,313