US2009131476A1PendingUtilityA1

Abuse-resistant amphetamine prodrugs

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Assignee: SHIRE LLCPriority: Feb 22, 2002Filed: Sep 26, 2008Published: May 21, 2009
Est. expiryFeb 22, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/30A61P 25/26A61P 25/34A61P 25/24A61P 3/04A61P 25/22A61P 25/08A61P 25/14A61P 25/00A61P 3/00A61P 25/20A61P 25/28A61P 25/16A61P 25/18C07C 237/06A61K 47/542Y10T436/173845A61P 15/10Y10S436/901A61K 31/165
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Claims

Abstract

The invention describes compounds, compositions, and methods of using the same comprising a chemical moiety covalently attached to amphetamine. These compounds and compositions are useful for reducing or preventing abuse and overdose of amphetamine. These compounds and compositions find particular use in providing an abuse-resistant alternative treatment for certain disorders, such as attention deficit hyperactivity disorder (ADHD), ADD, narcolepsy, and obesity. Oral bioavailability of amphetamine is maintained at therapeutically useful doses. At higher doses bioavailability is substantially reduced, thereby providing a method of reducing oral abuse liability. Further, compounds and compositions of the invention decrease the bioavailability of amphetamine by parenteral routes, such as intravenous or intranasal administration, further limiting their abuse liability.

Claims

exact text as granted — not AI-modified
1 . A composition comprising an amphetamine covalently bonded to a peptide comprising from 2 to 10 amino acids; wherein at least one of said amino acids is a naturally occurring amino acid and at least one of said amino acids is a non-naturally occurring amino acid; or a salt thereof. 
   
   
       2 . A composition as defined in  claim 1 , wherein said non-naturally occurring amino acid is selected from the group consisting of aminohexanoic acid, biphenylalanine, cyclohexylalanine, cyclohexylglycine, diethylglycine, dipropylglycine, 2,3-diaminoproprionic acid, homophenylalanine, homoserine, homotyrosine, naphthylalanine, norleucine, ornithine, phenylalanine (4-fluoro), phenylalanine(2,3,4,5,6-pentafluoro), phenylalanine(4-nitro), phenylglycine, pipecolic acid, sarcosine, tetrahydroisoquinoline-3-carboxylic acid, and tert-leucine. 
   
   
       3 . A composition as defined in  claim 2 , wherein said non-naturally occurring amino acid is selected from the group consisting of non-naturally occurring amino acids having a C 1 -C 6  alkyl side chains. 
   
   
       4 . A composition as defined in  claim 1 , wherein said amphetamine is selected from the group consisting of methylphenidate, methamphetamine, a compound having the formula 
     
       
         
         
             
             
         
       
     
     a salt of any of the foregoing, or a combination of any of the foregoing. 
   
   
       5 . A composition as defined in  claim 1 , wherein said composition is in a dosage form selected from the group consisting of a tablet, capsule, caplet, oral solution, and oral suspension. 
   
   
       6 . A composition as defined in  claim 5 , wherein said dosage form further comprises a pharmacological substance selected from the group consisting of amphetamines, antidepressants, anxiolytics, non-steroidal anti-inflammatory drugs, or any combination of any of the foregoing. 
   
   
       7 . A composition comprising an amphetamine covalently bonded to a peptide comprising from 2 to 10 amino acids; or a salt thereof wherein at least one of said amino acids is a naturally occurring amino acid and at least one of said amino acids is a non-naturally occurring amino acid and wherein said composition provides a therapeutically bioequivalent AUC of said amphetamine when compared to the AUC of said amphetamine when administered in a form in which said amphetamine is not covalently bonded to a peptide comprising from 2 to 10 amino acids. 
   
   
       8 . A method, in a subject in need thereof, of treating attention deficit hyperactivity disorder, said method comprising administering to said subject a composition as defined in  claim 1  or  7 .

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