US2013259832A1PendingUtilityA1

Combinations of Hepatitis C Virus Inhibitors

Assignee: BRISTOL MYERS SQUIBB COPriority: Oct 12, 2009Filed: Mar 11, 2013Published: Oct 3, 2013
Est. expiryOct 12, 2029(~3.2 yrs left)· nominal 20-yr term from priority
A61P 31/12A61P 31/14A61P 1/16A61K 38/06A61K 45/06C07D 403/14A61K 38/21A61K 31/4164A61K 31/4178A61K 31/4155A61K 31/4725A61K 2300/00C07D 403/12C07D 403/04
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Claims

Abstract

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit Hepatitis C virus (HCV), compositions comprising such compounds, and methods for treating Hepatitis C using such combinations.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A composition comprising a therapeutically effective amount of a compound of formula (I) 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, and a therapeutically effective amount of a compound of formula (II), 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 
     
     
         2 . The composition of  claim 1  further comprising one or two additional compounds having anti-HCV activity. 
     
     
         3 . The composition of  claim 2  wherein at least one of the additional compounds is an interferon or a ribavirin. 
     
     
         4 . The composition of  claim 3  wherein the interferon is selected from interferon alpha 2B, pegylated interferon alpha, consensus interferon, interferon alpha 2A, interferon lambda, pegylated interferon lambda, and lymphoblastoid interferon tau. 
     
     
         5 . A method of treating an HCV infection in a patient, comprising administering to the patient a therapeutically effective amount of a composition of  claim 1 . 
     
     
         6 . The method of  claim 5  further comprising administering one or two additional compound having anti-HCV activity prior to, after or simultaneously with the composition of  claim 1 . 
     
     
         7 . The method of  claim 6  wherein at least one of the additional compounds is an interferon or a ribavirin. 
     
     
         8 . The method of  claim 7  wherein the interferon is selected from interferon alpha 2B, pegylated interferon alpha, consensus interferon, interferon alpha 2A, interferon lambda, pegylated interferon lambda, and lymphoblastoid interferon tau.

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