US2012232004A1PendingUtilityA1

Methods for Treating Autoimmune Disorders, and Reagents Related Thereto

Individually held — no corporate assignee on recordPriority: Nov 26, 2001Filed: Mar 14, 2012Published: Sep 13, 2012
Est. expiryNov 26, 2021(expired)· nominal 20-yr term from priority
A61P 3/10A61P 37/00A61P 5/14A61P 43/00A61P 37/06A61P 37/02A61P 37/08A61P 31/18A61P 7/00A61P 25/00A61P 29/00A61P 17/00A61K 31/69A61K 31/401A61K 38/005A61P 13/12A61P 1/18A61P 1/04A61P 19/02A61P 1/00A61P 21/04A61P 19/04A61K 31/40
48
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Claims

Abstract

The invention generally relates to improved methods for the treatment or prophylaxis in animal subjects (including humans) of autoimmune disorders including Type I diabetes, septic shock, multiple sclerosis, inflammatory bowel disease (IBD) and Crohn's disease.

Claims

exact text as granted — not AI-modified
1 - 43 . (canceled) 
     
     
         44 . A method of treating an animal afflicted with Type 1 diabetes, comprising administering to said animal a therapeutically effective amount of a composition comprising an inhibitor of DPIV or a salt thereof in an amount sufficient to suppress the immune system, thereby slowing the rate of destruction of pancreatic beta cells. 
     
     
         45 . A method of treating an animal afflicted with Type 1 diabetes, comprising administering to said animal a therapeutically effective amount of a composition comprising an inhibitor of DPIV or a salt thereof in an amount sufficient to suppress the immune system, thereby stimulating β-cell growth and differentiation. 
     
     
         46 . The method of  claim 44  or  45 , wherein the inhibitor has a Ki of less than about 10 nM against DPIV. 
     
     
         47 . The method of  claim 44  or  45 , wherein the inhibitor has a Ki of less than about 1.0 nM against DPIV. 
     
     
         48 . The method of  claim 44  or  45 , wherein the inhibitor has a Ki of less than about 0.1 nM against DPIV. 
     
     
         49 . The method of  claim 44  or  45 , wherein the inhibitor has a Ki of less than about 0.01 nM against DPIV. 
     
     
         50 . A method of treating an animal afflicted with Type 1 diabetes, comprising administering to said animal a therapeutically effective amount of a composition comprising an inhibitor of DPIV or a salt thereof in an amount sufficient to suppress the immune system, thereby slowing the rate of destruction of pancreatic beta cells, wherein said inhibitor has an EC50 in the μM range or less. 
     
     
         51 . A method of treating an animal afflicted with Type 1 diabetes, comprising administering to said animal a therapeutically effective amount of a composition comprising an inhibitor of DPIV or a salt thereof in an amount sufficient to suppress the immune system, thereby stimulating β-cell growth and differentiation, wherein said inhibitor has an EC50 in the μM range or less. 
     
     
         52 . The method of  claim 50  or  51 , wherein the EC50 is in the nM range or less. 
     
     
         53 . The method of  claim 50  or  51 , wherein the EC50 is in the pM range or less. 
     
     
         54 . The method of  claim 44  or  45 , wherein said inhibitor of DPIV is a small molecule. 
     
     
         55 . The method of  claim 54 , wherein said small molecule has a molecular weight of less than 5000 amu. 
     
     
         56 . The method of  claim 54 , wherein said small molecule has a molecular weight of less than 2000 amu. 
     
     
         57 . The method of  claim 54 , wherein said small molecule has a molecular weight of less than 1000 amu. 
     
     
         58 . The method of  claim 44  or  45 , wherein said inhibitor of DPIV is a peptidomimetic. 
     
     
         59 . The method of  claim 44  or  45 , wherein said inhibitor of DPIV has insulinotropic activity. 
     
     
         60 . The method of  claim 44  or  45 , wherein said inhibitor of DPIV is orally active. 
     
     
         61 . The method of  claim 44  or  45 , wherein said animal is a human.

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