US2004204467A1PendingUtilityA1

Use of 5HT3-receptor-antagonists

Priority: Dec 22, 1998Filed: Apr 30, 2004Published: Oct 14, 2004
Est. expiryDec 22, 2018(expired)· nominal 20-yr term from priority
Inventors:Dieter Welzel
A61P 43/00A61P 25/20A61P 3/02A61P 29/00A61P 11/04A61P 21/00A61P 19/02A61K 31/415
48
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Claims

Abstract

A method of treatment for Chronic Fatigue Syndrome (CFS) comprising reducing the effect of serotonin by administering a dosage unit comprised of 5HT 3 -receptor-antagonist in an amount effective to decrease the effect of serotonin.

Claims

exact text as granted — not AI-modified
1 . A method of treatment for Chronic Fatigue Syndrome (CFS) comprising reducing the effect of serotonin by administering a dosage unit comprised of 5HT 3 -receptor-antagonist in an amount effective to decrease the effect of serotonin.  
     
     
         2 . The method of  claim 1 , wherein the 5HT 3 -receptor-antagonists is selected from the group consisting of Alosetron, Tropisetron, Ondansetron, Granisetron, Bemesetron, and mixtures thereof.  
     
     
         3 . The method of  claim 1 , wherein said administering step comprises administering said 5HT 3 -receptor-antagonist in an amount of 2 to 10 mg.  
     
     
         4 . The method of  claim 1 , wherein said administering step comprises administering a daily dosage of said 5HT 3 -receptor antagonist in an amount from 2 to 20 mg.  
     
     
         5 . The method of  claim 1 , wherein said 5HT 3 -receptor-antagonist is administered orally.  
     
     
         6 . The method of  claim 1 , wherein said administering said dosage unit comprises administering said dosage unit comprising Tropisetron.  
     
     
         7 . The method of  claim 6 , wherein said administering said dosage unit comprises administering said dosage unit comprising Tropisetron and at least one substance selected from the group consisting of Alosetron, Ondansetron, Granisetron, Bemesetron and combinations thereof.  
     
     
         8 . The method of  claim 1 , wherein said 5HT 3 -receptor-antagonist is administered intravenously.  
     
     
         9 . The method of  claim 3 , wherein said amount of said 5HT 3 -receptor-antagonist contained in said dosage unit is 5 to 8 mg.  
     
     
         10 . The method of  claim 4 , wherein said daily dosage of said 5HT 3 -receptor-antagonist comprises an amount of said 5HT 3 -receptor-antagonist from 5 to 16 mg.

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