US2006063840A1PendingUtilityA1

Use of a specific cyclic amine derivative or the pharmaceutically acceptable salts thereof for the treatment or prevention of heart failure

Assignee: BOEHRINGER INGELHEIM PHARMAPriority: Jul 25, 2002Filed: Nov 14, 2005Published: Mar 23, 2006
Est. expiryJul 25, 2022(expired)· nominal 20-yr term from priority
A61P 9/00A61K 9/0095A61K 31/195A61K 31/55A61K 45/06
55
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Claims

Abstract

The present invention provides the use in a pharmaceutical composition of a specific cyclic amine derivative, or its pharmaceutically acceptable salts, for the treatment of heart failure of any aetiology.

Claims

exact text as granted — not AI-modified
1 . A method of treating heart failure comprised of the steps of administering to a patient in need thereof a therapeutically effective amount of a pharmaceutical composition comprising cilobradine or a pharmaceutically acceptable salt thereof.  
   
   
       2 . The method of  claim 1  wherein the galenical formulation of the pharmaceutical composition is selected from a tablet, a drinking solution, a capsule, a suppository or an injectable formulation.  
   
   
       3 . The method of  claim 2  wherein the galenical formulation of the pharmaceutical composition is a tablet.  
   
   
       4 . The method of  claim 2  wherein the galenical formulation of the pharmaceutical composition is a drinking solution.  
   
   
       5 . The method of  claim 1  wherein the pharmaceutical composition is administered daily.  
   
   
       6 . The method of  claim 5  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.01 and 20 mg/kg body weight.  
   
   
       7 . The method of  claim 5  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.05 and 5 mg/kg body weight.  
   
   
       8 . The method of  claim 5  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 2.5 mg/kg body weight.  
   
   
       9 . The method according to  claim 5  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 1 mg/kg body weight.  
   
   
       10 . The method of  claim 5  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 0.75 mg/kg body weight.  
   
   
       11 . The method of  claim 1  wherein the treatment of heart failure is performed in combination with other therapeutic agents for the treatment of heart failure.  
   
   
       12 . The method of  claim 1   1  wherein said therapeutic agents include diuretics, cardiac glycosides, ACE inhibitors, ARBs, vasodilators, beta blockers or inotropes.  
   
   
       13 . The method of  claim 1  wherein the pharmaceutical composition is administered multiple times daily.  
   
   
       14 . The method of  claim 13  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.01 and 20 mg/kg body weight.  
   
   
       15 . The method of  claim 13  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.05 and 5 mg/kg body weight.  
   
   
       16 . The method of  claim 13  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 2.5 mg/kg body weight.  
   
   
       17 . The method according to  claim 13  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 1 mg/kg body weight.  
   
   
       18 . The method of  claim 13  wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 0.75 mg/kg body weight.

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