US2021188998A1PendingUtilityA1

Pharmaceutical composition for treatment and prevention of cancers

Assignee: TORAY INDUSTRIESPriority: Aug 5, 2008Filed: Feb 17, 2021Published: Jun 24, 2021
Est. expiryAug 5, 2028(~2 yrs left)· nominal 20-yr term from priority
C07K 2317/734A61P 15/00A61P 25/00A61K 2039/505C07K 2317/732C07K 2317/34C07K 16/3053C07K 16/3015C07K 2317/565C07K 16/30C07K 2317/24A61P 35/00C07K 2317/56A61P 1/04A61P 35/02A61K 39/39558A61P 11/00
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Claims

Abstract

The present invention relates to a pharmaceutical composition for treatment and/or prevention of cancer, which comprises, as an active ingredient, an antibody or fragment thereof having an immunological reactivity with a CAPRIN-1 protein or a fragment thereof comprising 7 or more consecutive amino acids.

Claims

exact text as granted — not AI-modified
1 . A method of preparing an antibody, comprising:
 administering a CAPRIN-1 protein, which has an amino acid sequence shown in any one of even-numbered SEQ ID NOs: 2 to 30, or a polypeptide fragment thereof, to a mammal to be immunized, and   purifying the resultant antibodies to obtain the antibody that specifically binds the CAPRIN-1 protein or a polypeptide fragment thereof expressed on the cell surface of a cancer and has an antitumor activity.   
     
     
         2 . The method according to  claim 1 , wherein the antitumor activity is an antibody-dependent cell-mediated cytotoxicity (ADCC) activity of the antibody. 
     
     
         3 . The method according to  claim 1 , wherein the antibody is a monoclonal antibody or polyclonal antibody. 
     
     
         4 . The method according to  claim 1 , wherein the antibody is a human antibody, a humanized antibody, a chimeric antibody, a single-chain antibody, or a bispecific antibody. 
     
     
         5 . The method according to  claim 1 , further comprising separating spleen cells from the immunized mammal and fusing the separated spleen cells with mammalian myeloma cells to obtain a hybridoma producing the antibody. 
     
     
         6 . The method according to  claim 5 , further comprising cloning DNA encoding an antibody from the hybridoma to obtain a clone for the antibody, incorporating the clone into a vector, and introducing the vector into a host cell to produce a recombinant antibody. 
     
     
         7 . The method according to  claim 6 , wherein the cloned DNA comprises DNA encoding a heavy chain variable region and a light chain variable region of the antibody. 
     
     
         8 . The method according to  claim 1 , further comprising preparing an antigen-binding fragment from the antibody, wherein the fragment specifically binds the CAPRIN-1 protein or polypeptide fragment thereof expressed on the cell surface of a cancer and has an antitumor activity.

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