US2016106727A1PendingUtilityA1

Composition and method for the treatment of neurodegeneration

Assignee: UNIV WRIGHT STATEPriority: Sep 12, 2011Filed: Dec 29, 2015Published: Apr 21, 2016
Est. expirySep 12, 2031(~5.1 yrs left)· nominal 20-yr term from priority
Inventors:Adrian Corbett
A61P 39/06A61K 31/375A61K 31/366A61K 31/4525A61P 25/28A61K 31/138
43
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Claims

Abstract

A composition and method for the treatment of neurodegeneration and brain-derived neurotrophic factor. The composition and method comprising providing paroxetine, simvastatin, and optionally, an antioxidant.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A composition for the treatment of neurodegeneration comprising:
 paroxetine; and   simvastatin.   
     
     
         2 . The composition of  claim 1  further comprising from about 0.81 mg/kg by weight of said paroxetine and from about 0.081 mg/kg by weight of said simvastatin. 
     
     
         3 . The composition of  claim 1  further comprising an antioxidant. 
     
     
         4 . The composition of  claim 3  further comprising from about 3.24 mg/kg by weight of said antioxidant. 
     
     
         5 . The composition of  claim 3  wherein said antioxidant is an ascorbic acid. 
     
     
         6 . A method for the treatment of neurodegeneration comprising:
 administering a composition comprising paroxetine and simvastatin.   
     
     
         7 . The method of  claim 6  further comprising administering a composition comprising from about 0.81 mg/kg by weight of said paroxetine and from about 0.081 mg/kg by weight of said simvastatin. 
     
     
         8 . The method of  claim 6  further comprising an antioxidant. 
     
     
         9 . The method of  claim 8  further comprising administering a composition comprising from about 3.24 mg/kg by weight of said antioxidant. 
     
     
         10 . The method of  claim 8  wherein said antioxidant is an ascorbic acid. 
     
     
         11 . The method of  claim 6  further comprising administering said composition between at least 20-26 hours after ischemic stroke induction and continuing for at least 31 days.

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