US2020317789A1PendingUtilityA1

Anti-pd-l1 antibodies and uses thereof

Assignee: I MAB BIOPHARMA US LTDPriority: Jun 13, 2016Filed: Jun 23, 2020Published: Oct 8, 2020
Est. expiryJun 13, 2036(~9.9 yrs left)· nominal 20-yr term from priority
A61K 2039/5158A61K 35/17C07K 2317/92C07K 2317/565C07K 2317/56C07K 2317/31C07K 16/2827C07K 2317/76C07K 2317/567C07K 2317/52C07K 2317/33C07K 2317/32C07K 2317/24C07K 2317/21A61P 35/02A61P 35/00A61P 31/22A61P 31/20A61P 31/18A61P 31/16A61P 31/14A61P 31/08A61P 31/06A61P 31/04A61K 2039/575A61K 2039/505G01N 33/575G01N 2333/70596
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Claims

Abstract

Provided are anti-PD-L1 antibodies or fragments thereof. The antibodies or fragments thereof specifically bind to the immunoglobulin C domain of the PD-L1 protein. In various example, the antibodies or fragments thereof include a VH CDR1 of SEQ ID NO: 1, a VH CDR2 of SEQ ID NO: 2, a VH CDR3 of SEQ ID NO: 3, a VL CDR1 of SEQ ID NO: 4, a VL CDR2 of SEQ ID NO: 5, and a VL CDR3 of SEQ ID NO: 6, or variants of each thereof. Methods of using the antibodies or fragments thereof for treating and diagnosing diseases such as cancer and infectious diseases are also provided.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for treating cancer in a human patient having a cancer cell that expresses, over-expresses, or is induced to express PD-L1, comprising inhibiting the interaction between the immunoglobulin C (Ig C) domain of the PD-L1 protein and PD-1 in the patient. 
     
     
         2 . The method of  claim 1 , wherein the interaction is inhibited by an anti-PD-L1 antibody or fragment thereof that specifically binds to the Ig C domain. 
     
     
         3 . The method of  claim 2 , wherein the anti-PD-L1 antibody or fragment thereof does not specifically bind to the immunoglobulin V (Ig V) domain of the PD-L1 protein. 
     
     
         4 . The method of  claim 3 , wherein anti-PD-L1 antibody or fragment thereof binds to amino acid residues Y134, K162, and N183 in the Ig C domain. 
     
     
         5 . The method of  claim 1 , wherein the antibody or fragment thereof is a humanized antibody or a fragment thereof. 
     
     
         6 . The method of  claim 1 , wherein the cancer is a solid tumor. 
     
     
         7 . The method of  claim 1 , wherein the cancer is selected from the group consisting of bladder cancer, liver cancer, colon cancer, rectal cancer, endometrial cancer, leukemia, lymphoma, pancreatic cancer, small cell lung cancer, non-small cell lung cancer, breast cancer, urethral cancer, head and neck cancer, gastrointestinal cancer, stomach cancer, oesophageal cancer, ovarian cancer, renal cancer, melanoma, prostate cancer and thyroid cancer.

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