US2007218033A1PendingUtilityA1

Composition and method of treating hepatitis C

Assignee: SHERMAN KENNETHPriority: Sep 13, 1991Filed: May 11, 2007Published: Sep 20, 2007
Est. expirySep 13, 2011(expired)· nominal 20-yr term from priority
A61P 37/00A61P 31/14A61P 31/12A61P 1/16A61K 38/2292
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Claims

Abstract

Compositions and methods of use for treating hepatitis C virus-infected mammals are disclosed. The compositions include one or more thymosins in combination with one or more interferons. Methods of treatment include use of thymosins together, or sequentially with interferon.

Claims

exact text as granted — not AI-modified
1 - 24 . (canceled)  
     
     
         25 . A composition comprising a pharmaceutical dosage unit of a pharmaceutically acceptable carrier, 900-1200 μg/m 2  of body surface area or 1500-1700 μg thymosin-α and/or fragments of thymosin-α in combination with 1-3 MU of at least one α-interferon, said pharmaceutical dosage unit being capable of promoting in vivo inactivation of hepatitis C virus when administered to mammals infected with said virus.  
     
     
         26 . The composition of  claim 25 , wherein said α-interferon is interferon α-2b.  
     
     
         27 . The composition of  claim 26 , wherein said interferon is recombinant interferon.  
     
     
         28 . The composition of  claim 25 , wherein said thymosin α is thymosin α-1.  
     
     
         29 . An anti-hepatitis C formulation comprising 900-1200 μg/m 2  of body surface area or 1500-1700 μg of at least one thymosin-α or fragment of thymosin-α, said thymosin fragment selected from the group consisting of C-terminal 4-28, C-terminal 15-28, N-terminal 1-8, N-terminal 1-14 and N-terminal 1-20, in combination with 1-3 MU of at least one α-interferon in a pharmaceutically acceptable carrier, for use in the treatment of a mammal infected with hepatitis C virus.  
     
     
         30 . The formulation of  claim 29 , wherein said thymosin is Thymosin α-1.  
     
     
         31 . The formulation of  claim 29 , wherein said α-interferon is interferon α-2b.  
     
     
         32 . The formulation of  claim 31 , wherein said interferon is recombinant interferon.  
     
     
         33 . The composition of  claim 25 , wherein said fragment of thymosin-α is selected from the group consisting of C-terminal 4-28 fragment, C-terminal 15-28 fragment, N-terminal 1-8 fragment, N-terminal 1-14 fragment and N-terminal 1-12 fragments.

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