Method of treating atherosclerosis in high triglyceride subjects

Abstract

The present invention provides a compound of Formula I for use in the treatment, amelioration and/or prevention of diseases and conditions associated with CETP activity, such as atherosclerosis and dyslipidemia, in a subject with high triglyceride level; wherein R 1 , X 1 , R 7 , R 5 , C, L and p are defined herein. The present invention further provides a combination of pharmacologically active agents for use in the treatment, amelioration and/or prevention of diseases and conditions associated with CETP activity, such as atherosclerosis and dyslipidemia, in a subject with high triglyceride levels.

What is claimed is: 
     
         1 - 40 . (canceled) 
     
     
         41 . A method of treating or ameliorating atherosclerosis by raising HDL-C and/or lowering LDL-C, in a subject comprising, administering to the subject a therapeutically effective amount of the following compound: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof, wherein the subject's triglyceride level is a fasting triglyceride level greater than 200 mg/dL. 
       
     
     
         42 . A method of treating atherosclerosis by raising HDL-C and/or lowering LDL-C comprising:
 a. selecting a subject with a fasting triglyceride level greater than 200 mg/dL; and   b. administering to said subject a therapeutically effective amount of a compound of the formula:   
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof. 
       
     
     
         43 . The method according to claim  1  or claim  2  further comprising administering at least one other therapeutic agent selected from: statin, cholesterol absorption inhibitor, apoA-I up-regulator/inducer, pre-beta HDL mimetic, ABCA1 stabilizer or inducer, LXR agonist, FXR agonist, phospholipid transfer protein (PLTP) inhibitor, aldosterone synthase inhibitor (ASI), fibric acid derivative, fish oil, DGAT1 inhibitor and endothelial lipase inhibitor, or a pharmaceutically acceptable salt thereof. 
     
     
         44 . The method according to claim  1  wherein the compound maintains greater than or equal to 50% inhibition of CETP inhibitory activity in subjects with high plasma triglycerides when compared to subject with normal plasma triglycerides. 
     
     
         45 . The method according to claim  2  wherein the compound maintains greater than or equal to 50% inhibition of CETP inhibitory activity in subjects with high plasma triglycerides when compared to subject with normal plasma triglycerides. 
     
     
         46 . The method of  claim 43 , wherein the at least one other therapeutic agent is a statin or a pharmaceutically acceptable salt thereof. 
     
     
         47 . The method of  claim 43 , wherein the at least one other therapeutic agent is a cholesterol absorption inhibitor or a pharmaceutically acceptable salt thereof. 
     
     
         48 . The method of  claim 43 , wherein the at least one other therapeutic agent is a apoA-I up-regulator/inducer or a pharmaceutically acceptable salt thereof. 
     
     
         49 . The method of  claim 43 , wherein the at least one other therapeutic agent is a pre-beta HDL mimetic or a pharmaceutically acceptable salt thereof. 
     
     
         50 . The method of  claim 43 , wherein the at least one other therapeutic agent is a ABCA1 stabilizer or inducer or a pharmaceutically acceptable salt thereof. 
     
     
         51 . The method of  claim 43 , wherein the at least one other therapeutic agent is a LXR agonist or a pharmaceutically acceptable salt thereof. 
     
     
         52 . The method of  claim 43 , wherein the at least one other therapeutic agent is a FXR agonist or a pharmaceutically acceptable salt thereof.