US2008090757A1PendingUtilityA1

Kahalalide Compositions for the Treatment of Psoriasis

Assignee: PHARMA MAR SAUPriority: Feb 26, 2003Filed: Dec 4, 2007Published: Apr 17, 2008
Est. expiryFeb 26, 2023(expired)· nominal 20-yr term from priority
A61P 35/00C07K 14/4748A61P 17/00C07K 7/56C07K 7/08A61K 38/00A61P 17/06
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Claims

Abstract

Kahalalide compounds, in particular kahalalide F, are of use in a method to treat a mammal suffering from skin disease such as psoriasis while avoiding toxicity and leading to clinical improvement.

Claims

exact text as granted — not AI-modified
1 . A method for treating psoriasis in a mammal comprising topically administering to the mammal an effective non-toxic amount of a kahalalide compound.  
     
     
         2 . A composition comprising a kahalalide compound and a pharmaceutically-acceptable carrier, wherein the composition further comprises one or more anti-psoriasis agents.  
     
     
         3 . A composition according to  claim 2 , wherein the one or more anti-psoriasis agents are selected from the group consisting of emollients, keratolytic agents, coal tar, anthralin, corticosteroids, and calpotriene.  
     
     
         4 . A composition according to  claim 2 , further comprising a photosensitizing agent.  
     
     
         5 . A composition according to  claim 4 , wherein the photosensitizing agent is selected from the group consisting of methoxsalen, methotrexate, etretinate, a corticosteroid, and cyclosporine.  
     
     
         6 . A composition according to  claim 2 , wherein the kahalalide compound is kahalalide F, a 4-methylhexyl analogue of kahalalide F, or a mixture thereof.  
     
     
         7 . A composition according to  claim 6 , wherein the kahalalide compound is kahalalide F.  
     
     
         8 . A composition according to  claim 2 , wherein the composition is a topical composition.  
     
     
         9 . A composition according to  claim 2 , wherein the composition is an intradermal composition.  
     
     
         10 . A composition according to  claim 2 , wherein the composition is an intravenous composition.

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