US2006275357A1PendingUtilityA1

Organic compounds

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Assignee: OOMURA TOMOYUKIPriority: Apr 8, 2003Filed: Apr 6, 2004Published: Dec 7, 2006
Est. expiryApr 8, 2023(expired)· nominal 20-yr term from priority
Inventors:Tomoyuki OomuraMadhusudhan PudipeddiColleen RueggerAlan Edward RoyceMasaki SasakiTokuhiro Tamura
A61P 37/02A61P 37/00A61P 37/06A61P 9/00A61P 41/00A61P 43/00A61P 31/12A61P 25/28A61P 29/00A61P 31/00A61P 25/00A61K 9/4858A61K 9/4866A61K 31/138A61K 31/145A61K 45/06A61K 31/135A61K 9/2013A61K 9/0053A61K 9/2018A61K 9/2054A61K 31/137A61K 47/10A61K 47/26A61K 9/20A61K 9/48
50
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Claims

Abstract

A solid pharmaceutical composition suitable for oral administration, comprising: (a) S1P receptor agonist; and (b) a sugar alcohol.

Claims

exact text as granted — not AI-modified
1 . A solid pharmaceutical composition suitable for oral administration, comprising: 
 (a) a S1P receptor agonist; and    (b) a sugar alcohol.    
   
   
       2 . A composition according to  claim 1 , wherein the S1P receptor agonist comprises 2-amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol or 2-amino-2-{2-[4-(1-oxo-5-phenylpentyl)-phenyl]ethyl}propane-1,3-diol or a pharmaceutically acceptable salt thereof.  
   
   
       3 . A composition according to  claim 1 , wherein the sugar alcohol comprises mannitol.  
   
   
       4 . A composition according to  claim 1 , further comprising a lubricant.  
   
   
       5 . A composition according to  claim 4 , wherein the lubricant comprises magnesium stearate.  
   
   
       6 . A composition according to  claim 1 , comprising 0.5 to 5% by weight of the S1P receptor agonist.  
   
   
       7 . A composition according to  claim 1 , comprising 90 to 99.5% by weight of the sugar alcohol.  
   
   
       8 . A composition according to  claim 1 , comprising 1.5 to 2.5% by weight of the lubricant.  
   
   
       9 . A composition according to  claim 1 , in the form of a tablet.  
   
   
       10 . A composition according to  claim 1  in the form of a capsule.

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