US2004087608A1PendingUtilityA1

Pharmaceuticals for neuropathic pain

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Assignee: YAMANOUCHI PHARMA CO LTDPriority: Aug 2, 1999Filed: Jun 26, 2003Published: May 6, 2004
Est. expiryAug 2, 2019(expired)· nominal 20-yr term from priority
A61P 25/00A61K 31/429A61K 31/00
47
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Claims

Abstract

This invention relates to pharmaceuticals for neuropathic pains comprising an mGluR1 receptor antagonist for systemic administration. Drugs efficacious in treating various neuropathic pain can be provided by the invention.

Claims

exact text as granted — not AI-modified
1 . A pharmaceutical composition for systemic administration for use in treating a neuropathic pain, which comprises a compound having mGluR1 antagonistic activity in an amount effective for improving the neuropathic pain and a pharmaceutically acceptable carrier.  
     
     
         2 . The pharmaceutical composition according to  claim 1 , wherein the neuropathic pain is a neuropathic pain induced by diabetes or compression of nerves.  
     
     
         3 . The pharmaceutical composition according to  claim 2 , wherein the neuropathic pain is a neuropathic pain induced by diabetes.  
     
     
         4 . The pharmaceutical composition according to  claim 1 , wherein the systemic administration method is oral administration.  
     
     
         5 . The pharmaceutical composition according to  claim 1 , wherein the compound having mGluR1 antagonistic activity is a compound having sufficient mGluR1 antagonism for expressing neuropathic pain improving effect by systemic administration.  
     
     
         6 . The pharmaceutical composition according to  claim 1 , wherein the compound having mGluR1 antagonism is a compound selected from 6-amino-N-cyclohexyl-N,3-dimethylthiazolo[3,2-a]benzoimidazole-2-carboxamide dihydrochloride and (+)-(1R,2S)-6-amino-N-methyl-N-(2-methylcyclohexyl)thiazolo[3,2-a]benzoimidazole-2-carboxamide dihydrochloride.

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