US2019142939A1PendingUtilityA1

Combination therapy for inducing immune response to disease

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Assignee: IBC PHARMACEUTICALS INCPriority: Aug 14, 2012Filed: Jan 18, 2019Published: May 16, 2019
Est. expiryAug 14, 2032(~6.1 yrs left)· nominal 20-yr term from priority
A61K 38/212C07K 16/44C07K 16/3007A61K 47/6851C07K 2317/54C07K 16/2887A61K 47/6879C07K 16/30C07K 16/32A61K 39/39558C07K 2317/31C07K 16/2803C07K 16/2863A61K 2039/505C07K 16/2833A61K 38/21A61K 45/06A61K 47/6803C07K 16/2809A61K 47/68037C07K 2317/76C07K 2317/73C07K 2317/622C07K 2317/55
68
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Claims

Abstract

The present invention concerns compositions and methods of use of bispecific antibodies comprising at least one binding site for Trop-2 (EGP-1) and at least one binding site for CD3. The bispecific antibodies are of use for inducing an immune response against a Trop-2 expressing tumor, such as carcinoma of the esophagus, pancreas, lung, stomach, colon, rectum, urinary bladder, breast, ovary, uterus, kidney or prostate. The methods may comprising administering the bispecific antibody alone, or with one or more therapeutic agents such as antibody-drug conjugates, interferons (preferably interferon-α), and/or checkpoint inhibitor antibodies. The bispecific antibody is capable of targeting effector T cells, NK cells, monocytes or neutrophils to induce leukocyte-mediated cytotoxicity of Trop-2 + cancer cells. The cytotoxic immune response is enhanced by co-administration of interferon, checkpoint inhibitor antibody and/or ADC.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A composition comprising a bispecific antibody that comprises:
 a) a first antibody moiety that binds to human CD3, conjugated to an AD (anchoring domain) moiety from an AKAP protein; and   b) a second antibody moiety that binds to human CEACAM5, conjugated to a DDD (dimerization and docking domain) moiety, wherein the amino acid sequence of said DDD moiety is residues 1-44 of human protein kinase A (PKA) RIIa;   
       wherein two copies of the DDD moiety form a dimer that binds to one copy of the AD moiety to form the bispecific antibody. 
     
     
         2 . The composition of  claim 1 , wherein the bispecific antibody comprises at least one antibody fragment selected from the group consisting of a scFv, a Fab and a dAb. 
     
     
         3 . The composition of  claim 1 , wherein the second antibody moiety comprises a humanized MN-14 (anti-CEACAM5) antibody or antigen-binding fragment thereof. 
     
     
         4 . The composition of  claim 1 , wherein the first antibody moiety comprises an Okt3 (anti-CD3) antibody or antigen-binding fragment thereof. 
     
     
         5 . A bispecific antibody comprising
 a) a first antibody moiety that binds to human CD3, conjugated to an AD (anchoring domain) moiety from an AKAP protein; and   b) a second antibody moiety that binds to human Trop-2, conjugated to a DDD (dimerization and docking domain) moiety, wherein the amino acid sequence of said DDD moiety is residues 1-44 of human protein kinase A (PKA) RIIa;   
       wherein two copies of the DDD moiety form a dimer that binds to one copy of the AD moiety to form the bispecific antibody. 
     
     
         6 . The bispecific antibody of  claim 5 , wherein the second antibody moiety comprises a humanized MN-14 (anti-CEACAM5) antibody or antigen-binding fragment thereof. 
     
     
         7 . The bispecific antibody of  claim 5 , wherein the first antibody moiety comprises an Okt3 (anti-CD3) antibody or antigen-binding fragment thereof. 
     
     
         8 . The bispecific antibody of  claim 5 , wherein the bispecific antibody comprises at least one antibody fragment selected from the group consisting of an scFv, a Fab and a dAb.

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