US2006013887A1PendingUtilityA1

Delayed release carnitine

Individually held — no corporate assignee on recordPriority: Jun 16, 1993Filed: Sep 9, 2005Published: Jan 19, 2006
Est. expiryJun 16, 2013(expired)· nominal 20-yr term from priority
A61K 9/1652A61K 9/2077A61K 9/5042A61K 31/565A61K 31/205A61K 9/5026A61K 9/1635
58
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Claims

Abstract

A sustained release, orally administered pharmaceutical composition comprising carnitine and an acceptable pharmaceutical excipient is described for the treatment of carnitine deficiency and other carnitine responsive conditions. The sustained release formulation avoids the characteristic problems of gastrointestinal invitation, dumping in the urine and bacterial degradation attendant previously known oral formulations of carnitine.

Claims

exact text as granted — not AI-modified
1 - 14 . (canceled)  
   
   
       15 . A sustained release oral medicament for administration to a human being, the human being having gastrointestinal fluid, the medicament comprising: 
 (a) a unitary dosage amount of L-carnitine formed into granules;    (b) a coating of about 39% by weight of a copolymer synthesized from methacrylic acid esters with quaternary ammonium groups, wherein the molar ratio of the ammonium groups to the methacrylic acid esters is 1:40; and    (c) an acceptable pharmaceutical excipient.    
   
   
       16 . The sustained release oral medicament of  claim 15 , wherein the granules have a dimension of 20 mesh.  
   
   
       17 . The sustained release oral medicament of  claim 15 , wherein the granules have a dimension of 25-30 mesh.  
   
   
       18 . The sustained release oral medicament as claimed in  claim 15 , wherein the carnitine is slowly released over a period of time greater than two hours upon exposure to gastrointestinal fluid.

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