US2013023547A1PendingUtilityA1

Dispersible tablet

Assignee: HOLMAN LOVELACEPriority: May 17, 2005Filed: Sep 27, 2012Published: Jan 24, 2013
Est. expiryMay 17, 2025(expired)· nominal 20-yr term from priority
A61P 9/12A61P 11/00A61K 9/0095A61K 9/2095A61K 31/513A61K 9/20
46
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Claims

Abstract

The invention relates to dispersible tablets comprising the compound 4-tert-butyl-N-[6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-(pyrimidin-2-yl)-pyrimidin-4-yl]-benzenesulfonamide.

Claims

exact text as granted — not AI-modified
1 . A dispersible tablet comprising compound I of the formula 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt or solvate thereof, and pharmaceutically acceptable excipients, wherein the dispersible tablet disintegrates completely in water at 15-22° C. in not more than 5 minutes. 
       
     
     
         2 . The dispersible tablet according to  claim 1  comprising the following pharmaceutically acceptable excipients: a) at least one filler and b) at least one lubricant. 
     
     
         3 . The dispersible tablet according to  claim 2  further comprising at least one disintegrant. 
     
     
         4 . The dispersible tablet according to  claim 1  comprising at least one acidifying agent and/or at least one flavouring agent and/or at least one sweetening agent. 
     
     
         5 . The dispersible tablet according to  claim 1  comprising the following pharmaceutically acceptable excipients: one or more fillers in a total amount of 40 to 85% in weight based on the total weight of the dispersible tablet, one or more disintegrants in a total amount of 0.5 to 20% in weight based on the total weight of the dispersible tablet, one or more glidants in a total amount of 0.1 to 5% in weight based on the total weight of the dispersible tablet, one or more acidifying agents in a total amount of 0.5 to 13% in weight based on the total weight of the dispersible tablet, one or more flavouring agents in a total amount of 1 to 15% in weight based on the total weight of the dispersible tablet, one or more sweetening agents in a total amount of 0.1 to 10% in weight based on the total weight of the dispersible tablet, and one or more lubricants in a total amount of 0.05 to 7% in weight based on the total weight of the dispersible tablet. 
     
     
         6 . The dispersible tablet according to any one of the preceding claims wherein compound I is in the monohydrate form. 
     
     
         7 . The dispersible tablet according to any one of the preceding claims obtainable by using the method of direct compression. 
     
     
         8 . (canceled) 
     
     
         9 . A method for treating pulmonary arterial hypertension, comprising dispersing the dispersible tablet of  claim 1  in aqueous media to form a suspension and administering the suspension to a patient in need thereof. 
     
     
         10 . A process for the preparation of a dispersible tablet according to  claim 1 , characterized in that the tablet is prepared by direct compression. 
     
     
         11 . The dispersible tablet of  claim 1 , wherein the pharmaceutically acceptable excipients include a flavoring agent and/or a sweetener.

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