IP Library Granted Patent US 7,132,415
Granted Patent B2
US 7,132,415 · App. 10/247,095 · Granted Nov 7, 2006

Methods and therapeutic combinations for the treatment of xanthoma using sterol absorption inhibitors

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Quick Facts
Patent No.
US 7,132,415
App. No.
10/247,095
Granted
Nov 7, 2006
Kind
B2
Abstract

The present invention provides therapeutic combinations and methods including at least one sterol or 5α-stanol absorption inhibitor that can be useful for treating xanthomas.

Claims (15)

1. A method of decreasing the incidence of xanthoma in a subject comprising the step of administering to a subject in need of such treatment an effective amount of a combination of (i) at least one sterol absorption inhibitor, at least one 5α-stanol absorption inhibitor, or a pharmaceutically acceptable salt or solvate thereof and (ii) at least one HMG-CoA reductase inhibitor as a cholesterol biosynthesis inhibitor, to decrease the incidence of xanthoma in the subject, wherein the at least one sterol or 5α-stanol absorption inhibitor is represented by Formula (I):

or a pharmaceutically acceptable salt thereof or a solvate thereof, wherein:

Ar 1 and Ar 2 are independently selected from the group consisting of aryl and R 4 -substituted aryl;

Ar 3 is aryl or R 5 -substituted aryl;

X, Y and Z are independently selected from the group consisting of —CH 2 —, —CH(lower alkyl)- and —C(dilower alkyl)-;

R and R 2 are independently selected from the group consisting of —OR 6 , —O(CO)R 6 , —O(CO)OR 9 and —O(CO)NR 6 R 7 ;

R 1 and R 3 are independently selected from the group consisting of hydrogen, lower alkyl and aryl;

q is 0 or 1;

r is 0 or 1;

m, n and p are independently selected from 0, 1, 2, 3 or 4; provided that at least one of q and r is 1, and the sum of m, n, p, q and r is 1, 2, 3, 4, 5 or 6; and provided that when p is 0 and r is 1, the sum of m, q and n is 1, 2, 3, 4 or 5;

R 4 is 1–5 substituents independently selected from the group consisting of lower alkyl, —OR 6 , —O(CO)R 6 , —O(CO)OR 9 , —O(CH 2 ) 1-5 OR 6 , —O(CO)NR 6 R 7 , —NR 6 R 7 , —NR 6 (CO)R 7 , —NR 6 (CO)OR 9 , —NR 6 (CO)NR 7 R 8 , —NR 6 SO 2 R 9 , —COOR 6 , —CONR 6 R 7 , —COR 6 , —SO 2 NR 6 R 7 , S(O) 0-2 R 9 , —O(CH 2 ) 1-10 —COOR 6 , —O(CH 2 ) 1-10 CONR 6 R 7 , -(lower alkylene)COOR 6 , —CH═CH—COOR 6 , —CF 3 , —CN, —NO 2 and halogen;

R 5 is 1–5 substituents independently selected from the group consisting of —OR 6 , —O(CO)R 6 , —O(CO)OR 9 , —O(CH 2 ) 1-5 OR 6 , —O(CO)NR 6 R 7 , —NR 6 R 7 , —NR 6 (CO)R 7 , —NR 6 (CO)OR 9 , —NR 6 (CO)NR 7 R 8 , —NR 6 SO 2 R 9 , —COOR 6 , —CONR 6 R 7 , —COR 6 , —SO 2 NR 6 R 7 , S(O) 0-2 R 9 , —O(CH 2 ) 1-10 —COOR 6 , —O(CH 2 ), 1-10 CONR 6 R 7 , -(lower alkylene)COOR 6 and —CH═CH—COOR 6 ;

R 6 , R 7 and R 8 are independently selected from the group consisting of hydrogen, lower alkyl, aryl and aryl-substituted lower alkyl; and

R 9 is lower alkyl, aryl or aryl-substituted lower alkyl.

2. The method according to claim 1 , wherein the HMG-CoA reductase inhibitor is selected from the group consisting of pravastatin, lovastatin, simvastatin, fluvastatin, rivastatin, rosuvastatin, atorvastatin, cerivastatin, and combinations thereof.

Assignments (1)
CHANGE OF NAME Recorded Aug 30, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028884/0151 →