US2022089739A1PendingUtilityA1

Antibodies Directed Against Programmed Death-1 (PD-1)

Assignee: TESARO INCPriority: Nov 1, 2016Filed: Sep 27, 2021Published: Mar 24, 2022
Est. expiryNov 1, 2036(~10.3 yrs left)· nominal 20-yr term from priority
A61P 31/14A61P 37/02C07K 2317/33A61P 31/20C12N 15/63Y02A50/30A61K 39/3955A61P 31/00A61K 2039/505A61P 43/00A61P 3/10C07K 2317/76C07K 16/2803A61P 35/02A61P 17/00A61P 19/02A61P 37/04A61P 29/00C07K 2317/92C07K 2317/524A61P 35/00A61P 31/12C07K 2317/53A61P 1/04C07K 2317/41A61P 31/18C07K 16/2818A61P 25/00A61K 45/06A61P 31/16A61P 31/04A61P 17/06C07K 2317/56
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Claims

Abstract

The disclosure provides antibody agents that bind to a programmed death-1 (PD-1) protein. Particular immunoglobulin heavy chain polypeptide and immunoglobulin light chain polypeptide sequences are explicitly provided. Also provided are related nucleic acids, vectors, compositions, and methods of using the anti-PD-1 antibody agent to treat a disorder or disease that is responsive to PD-1 inhibition, such as cancer or an infectious disease.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating a disorder in a human that is responsive to PD-1 inhibition, the method comprising administering to the human an effective amount of an antibody comprising: a heavy chain polypeptide comprising the amino acid sequence of SEQ ID NO: 1 and a light chain polypeptide comprising the amino acid sequence of SEQ ID NO: 2, whereupon the disorder is treated in the human. 
     
     
         2 . The method of  claim 1 , wherein the disorder is cancer. 
     
     
         3 . The method of  claim 2 , wherein the cancer is: adenocarcinoma, endometrial cancer, breast cancer, ovarian cancer, cervical cancer, fallopian tube cancer, testicular cancer, primary peritoneal cancer, colon cancer, colorectal cancer, stomach cancer, small intestine cancer, squamous cell carcinoma of the anogenital region, melanoma, renal cell carcinoma, lung cancer, non-small cell lung cancer, adenocarcinoma of the lung, squamous cell carcinoma of the lung, stomach cancer, bladder cancer, gall bladder cancer, liver cancer, thyroid cancer, laryngeal cancer, salivary gland cancer, esophageal cancer, head and neck cancer, squamous cell carcinoma of the head and neck, prostate cancer, pancreatic cancer, mesothelioma, Merkel cell carcinoma, sarcoma, glioblastoma, and a hematological cancer, such as multiple myeloma, B-cell lymphoma, T-cell lymphoma, Hodgkin's lymphoma/primary mediastinal B-cell lymphoma, or chronic myelogenous leukemia. 
     
     
         4 . The method of  claim 2 , wherein the cancer: is characterized by microsatellite instability, is microsatellite instability high (MSI-H), has high tumor mutational burden (TMB), has a defective DNA mismatch repair system, has a defect in a DNA mismatch repair gene, is a hypermutated cancer, or comprises a mutation in polymerase epsilon (POLE).

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