US2006106110A1PendingUtilityA1

Modified amino acid for the inhibition of platelet aggregation

Assignee: BATEMAN SIMON DPriority: Jul 17, 2002Filed: Jul 16, 2003Published: May 18, 2006
Est. expiryJul 17, 2022(expired)· nominal 20-yr term from priority
A61K 38/23A61K 38/28A61K 38/29A61P 7/02A61K 31/727A61K 31/198A61K 31/166
61
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Claims

Abstract

A method of inhibiting blood platelet aggregation in a mammal is provided. The method comprises the administration of a platelet aggregation inhibiting amount of a modified amino acid or pharmaceutically acceptable salt thereof.

Claims

exact text as granted — not AI-modified
1 - 13 . (canceled)  
     
     
         14 . A method of inhibiting platelet aggregation in a mammal comprising administering a platelet inhibiting amount of a modified amino acid, or a pharmaceutically acceptable salt thereof.  
     
     
         15 . The method of  claim 14 , wherein the modified amino acid is N-(-5-chlorosalicyloyl)-8-aminocaprylic acid (5-CNAC), or a pharmaceutically acceptable salt thereof.  
     
     
         16 . The method of  claim 14 , wherein the modified amino acid is present in an amount of about 25 mg to about 400 mg.  
     
     
         17 . The method of  claim 14 , wherein the modified amino acid is present in an amount of about 100 mg to about 200 mg.  
     
     
         18 . The method of  claim 14 , wherein the method further comprises administering a pharmacologically active agent with said modified amino acid, or pharmaceutically acceptable salt thereof, wherein the modified amino acid or salt thereof is present in an amount effective to inhibit platelet aggregation.  
     
     
         19 . The method of  claim 18 , wherein the modified amino acid is N-(-5-chlorosalicyloyl)-8-aminocaprylic acid (5-CNAC), or a pharmaceutically acceptable salt thereof.  
     
     
         20 . The method of  claim 19 , wherein the pharmacologically active agent comprises heparin, insulin, parathyroid hormone or calcitonin.  
     
     
         21 . The method of  claim 20 , wherein the mammal is human and the calcitonin is salmon calcitonin.  
     
     
         22 . The method of  claim 18 , wherein the pharmacologically active agent is present in an amount of 0.05% to 70% by weight relative to the total weight of the pharmaceutical composition.  
     
     
         23 . The method of  claim 18  wherein the pharmaceutical composition comprises calcitonin and 5-CNAC or a pharmaceutically acceptable salt thereof.  
     
     
         24 . A pharmaceutical composition comprising a platelet aggregation inhibiting amount of a modified amino acid, or a pharmaceutically acceptable salt thereof.  
     
     
         25 . The composition of  claim 24 , further comprising a pharmacologically active agent and a modified amino acid, or pharmaceutically acceptable salt thereof, wherein the modified amino acid or salt thereof is present in an amount effective to inhibit platelet aggregation.

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