US2007092566A1PendingUtilityA1

Oral sustained-release tablet

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Assignee: HOSHINO RYOUICHIPriority: Aug 4, 2003Filed: Aug 3, 2004Published: Apr 26, 2007
Est. expiryAug 4, 2023(expired)· nominal 20-yr term from priority
A61P 43/00A61K 9/2054A61P 13/02A61K 31/4174A61P 13/00A61K 47/38A61K 9/20
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Claims

Abstract

An oral sustained-release tablet is provided, which does not cause initial rapid increases in the bloodlevels of 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutylamide (KRP-197) and can maintain constant the blood levels. (Solving means) An oral sustained-release tablet comprises a pharmaceutical composition and a gel-forming material, the pharmaceutical composition containing KRP-197 as an active ingredient.

Claims

exact text as granted — not AI-modified
1 . An oral sustained-release tablet comprising a pharmaceutical composition and a gel-forming material, the pharmaceutical composition containing 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutylamide as an active ingredient.  
   
   
       2 . The oral sustained-release tablet according to  claim 1 , wherein the gel-forming material is hydroxypropylmethylcellulose.  
   
   
       3 . The oral sustained-release tablet according to  claim 1 , wherein the pharmaceutical composition contains 18 to 73 wt % of hydroxypropylmethylcellulose.  
   
   
       4 . The oral sustained-release tablet according to  claim 1 , obtained by mixing a granular composition containing 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutylamide with a composition containing a gel-forming material.  
   
   
       5 . The oral sustained-release tablet according to  claim 4 , wherein 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutylamide containing granules are manufactured by using a solution of 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutylamide.

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