US2014044707A1PendingUtilityA1

ANTIBODIES THAT BIND HUMAN PROTEIN TYROSINE PHOSPHATASE beta (HPTPbeta) AND USES TEHREOF

Assignee: AERPIO THERAPEUTICS INCPriority: Apr 7, 2006Filed: Aug 5, 2013Published: Feb 13, 2014
Est. expiryApr 7, 2026(expired)· nominal 20-yr term from priority
A61P 37/04A61P 37/00A61P 43/00A61P 9/12A61P 9/10A61P 7/06A61P 9/00A61P 9/08A61P 3/10A61P 27/02A61P 35/02A61P 31/18A61P 31/04A61P 35/00A61P 25/02A61P 29/00A61P 33/02C07K 2317/75C07K 2317/73C07K 2317/55A61P 11/00A61P 1/02C07K 16/28A61P 1/04C07K 16/40A61P 13/12A61K 2039/505A61P 17/06A61P 17/00A61P 19/08A61P 19/02C07K 16/18A61P 17/02C07K 2317/76C07K 2317/24C07K 2317/56C07K 2317/54A61P 1/00A61K 39/395
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Claims

Abstract

Antibodies and antigen binding fragments thereof that bind to human protein tyrosine phosphatase beta (HPTPβ), and uses thereof.

Claims

exact text as granted — not AI-modified
1 .- 24 . (canceled) 
     
     
         25 . A method of treating an angiogenesis regulated disorder in a subject, comprising:
 a) identifying a subject in need of regulation of angiogenesis; and   b) administering to the subject an effective amount of an antibody or antigen-binging fragment thereof which binds HPTPbeta and regulates angiogenesis.   
     
     
         26 . The method according to  claim 25 , wherein angiogenesis regulated disorder is an angiogenesis elevated disorder selected from the group consisting of cancer, sickle cell anemia, sarcoid, syphilis, pseudoxanthoma elasticum, Paget's disease, mycobacterial infections, Lyme's disease, systemic lupus erythematosis, Eales' discease, Behcet's disease, Best's disease, Stargardt's disease, pars planitis, hyperviscosity syndrome, toxoplasmosis, trauma and post-laser complications, and diseases associated with rubeosis. 
     
     
         27 . The method according to  claim 26 , wherein the antibody binds the N-terminal portion of HPTPβ. 
     
     
         28 . The method according to  claim 26 , wherein the antibody binds the first FN3 repeat of HPTPβ. 
     
     
         29 . The method according to  claim 28 , wherein the first FN3 repeat of HPTPβ has the sequence as shown in SEQ ID NO: 11, or a fragment thereof. 
     
     
         30 . The method according to  claim 26 , wherein the antibody is a monoclonal antibody. 
     
     
         31 . The method according to  claim 30 , wherein the monoclonal antibody is produced by hybridoma cell line ATCC No. PTA-7580 or a fragment of a monoclonal antibody according to  claim 30 , produced by hybridoma cell line ATCC No. PTA-7580. 
     
     
         32 . The method according to  claim 31 , wherein the antibody or an antigen binding fragment is humanized. 
     
     
         33 . The method according to  claim 26 , wherein the antibody binding fragment comprises heavy and light chain variable regions. 
     
     
         34 . The method according to  claim 33 , wherein the antigen-binding fragment is selected from the group consisting of an Fv fragment, an Fab fragment, an Fab′ fragment, and an F(ab′) 2  fragment. 
     
     
         35 . The method according to  claim 25 , wherein angiogenesis regulated disorder is an angiogenesis elevated disorder selected from the group consisting of inflammatory bowel diseases including Crohn's disease and ulcerative colitis, psoriasis, sarcoidosis, and rheumatoid arthritis. 
     
     
         36 . The method according to  claim 35 , wherein the antibody binds the N-terminal portion of HPTPβ. 
     
     
         37 . The method according to  claim 35 , wherein the antibody binds the first FN3 repeat of HPTPβ. 
     
     
         38 . The method according to  claim 37 , wherein the first FN3 repeat of HPTPβ has the sequence as shown in SEQ ID NO: 11, or a fragment thereof. 
     
     
         39 . The method according to  claim 35 , wherein the antibody is a monoclonal antibody. 
     
     
         40 . The method according to  claim 39 , wherein the monoclonal antibody is produced by hybridoma cell line ATCC No. PTA-7580 or a fragment of a monoclonal antibody according to  claim 30 , produced by hybridoma cell line ATCC No. PTA-7580. 
     
     
         41 . The method according to  claim 40 , wherein the antibody or an antigen binding fragment is humanized. 
     
     
         42 . The method according to  claim 35 , wherein the antibody binding fragment comprises heavy and light chain variable regions. 
     
     
         43 . The method according to  claim 40 , wherein the antigen-binding fragment is selected from the group consisting of an Fv fragment, an Fab fragment, an Fab′ fragment, and an F(ab′) 2  fragment.

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