US2007208075A1PendingUtilityA1

Pharmaceutical compositions

Assignee: COTTENS SYLVAINPriority: Oct 26, 1994Filed: Mar 8, 2007Published: Sep 6, 2007
Est. expiryOct 26, 2014(expired)· nominal 20-yr term from priority
A61K 9/1075A61K 31/4745A61K 38/13A61K 31/365A61K 31/19A61K 9/4858A61K 9/0095
64
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Claims

Abstract

This invention provides a microemulsion pre-concentrate comprising a difficultly soluble active agent and a carrier medium comprising 1) a hydrophilic phase which comprises dimethylisosorbide and/or a lower alkyl alkanoic ester, 2) a lipophilic phase, and 3) a surfactant. The active agent may be a cyclosporin or a macrolide. In another aspect, this invention provides a pharmaceutical composition for enteral or parenteral administration comprising a macrolide and an acid.

Claims

exact text as granted — not AI-modified
1 - 5 . (canceled)  
   
   
       6 . A pharmaceutical composition for enteral or parenteral administration comprising a macrolide and an acid.  
   
   
       7 . A composition as claimed in  claim 6  wherein the acid is a mono-, di-, or tri-carboxylic acid.  
   
   
       8 . A composition as claimed in  claim 6  wherein the acid is selected from malonic acid, oxalic acid, citric acid and lactic acid.  
   
   
       9 . Use of an acid to stabilize a macrolide in a pharmaceutical composition.  
   
   
       10 . A method of stabilizing a macrolide in a pharmaceutical composition, which method comprises mixing an acid with the macrolide.

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