The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 12, 2022

Filed:

Nov. 20, 2017
Applicants:

Memorial Sloan-kettering Cancer Center, New York, NY (US);

Eureka Therapeutics, Inc., Emeryville, CA (US);

Inventors:

David A. Scheinberg, New York, NY (US);

Tao Dao, New York, NY (US);

Cheng Liu, Emeryville, CA (US);

Hong Liu, El Sobrante, CA (US);

Yiyang Xu, Pleasanton, CA (US);

Su Yan, State College, PA (US);

Assignees:

MEMORIAL SLOAN-KETTERING CANCER CENTER, New York, NY (US);

EUREKA THERAPEUTICS, INC., Emeryville, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07K 16/30 (2006.01); C07K 16/46 (2006.01); C07K 16/28 (2006.01); A61K 47/68 (2017.01); G01N 33/574 (2006.01); A61K 39/00 (2006.01); C07K 14/00 (2006.01);
U.S. Cl.
CPC ...
C07K 16/28 (2013.01); A61K 47/6849 (2017.08); C07K 16/2809 (2013.01); C07K 16/2833 (2013.01); C07K 16/30 (2013.01); C07K 16/3053 (2013.01); G01N 33/57492 (2013.01); A61K 39/0011 (2013.01); A61K 2039/505 (2013.01); A61K 2039/5156 (2013.01); A61K 2039/5158 (2013.01); C07K 14/00 (2013.01); C07K 2317/21 (2013.01); C07K 2317/31 (2013.01); C07K 2317/32 (2013.01); C07K 2317/34 (2013.01); C07K 2317/41 (2013.01); C07K 2317/56 (2013.01); C07K 2317/565 (2013.01); C07K 2317/622 (2013.01); C07K 2317/732 (2013.01); C07K 2319/03 (2013.01); C07K 2319/33 (2013.01); C07K 2319/74 (2013.01); G01N 2333/705 (2013.01);
Abstract

The presently disclosed subject matter provides antigen-binding proteins that specifically bind to Preferentially expressed antigen of melanoma (PRAME), including humanized, chimeric and fully human antibodies against PRAME, antibody fragments (e.g., scFv, Fab and F(ab)), chimeric antigen receptors (CARs), fusion proteins, and conjugates thereof. The antigen-binding proteins and antibodies bind to a PRAME peptide/HLA class I molecule complex. Such antibodies, fragments, fusion proteins and conjugates thereof are useful for the treatment of PRAME associated diseases, including for example, breast cancer, ovarian cancer, melanoma, lung cancer, gastrointestinal cancer, brain tumor, head and neck cancer, renal cancer, myeloma, neuroblastoma, mantle cell lymphoma, chronic myelocytic leukemia, multiple myeloma, acute lymphoblastic leukemia (ALL), acute myeloid/myelogenous leukemia (AML), Non-Hodgkin lymphoma (NHL), and Chronic lymphocytic leukemia (CLL). The antibodies or antigen binding proteins may comprise one or more framework region amino acid substitutions designed to improve protein stability, antibody binding and/or expression levels.


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