IP Library Granted Patent US 7,179,792
Granted Patent B2
US 7,179,792 · App. 10/699,967 · Granted Feb 20, 2007

Combination product of a 1,4-benzothiepine 1,1-dioxide compound with at least one other active ingredient and the use of the product

Assignee: Sanofi-Aventis Deulschland GmbH
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Quick Facts
Patent No.
US 7,179,792
App. No.
10/699,967
Granted
Feb 20, 2007
Kind
B2
Abstract

The present invention is directed to a 1,4-benzothiepine 1,1-dioxide compound of formula I in which the radicals have the meanings defined herein, or a pharmaceutically acceptable salt or physiologically functional derivative thereof, with at least one other active ingredient, or a pharmaceutically acceptable salt or physiologically functional derivative thereof. The invention is also directed to the use of the combination product, pharmaceutical composition comprising the combination product and method for preparing the pharmaceutical composition.

Claims (51)

1. A method for effecting the or treatment of a lipid metabolism disorder or metabolic syndrome in a patient comprising administering a pharmaceutically effective amount of a composition of matter comprising a compound of formula I

in which

R 1 is methyl, ethyl, propyl, or butyl;

R 2 is H, —OH, —NH 2 , or —NH—(C 1 –C 6 )-alkyl;

R 3 is a saccharide residue, disaccharide residue, trisaccharide residue, or tetrasaccharide residue, wherein the saccharide residue, disaccharide residue, trisaccharide residue or tetrasaccharide residue is optionally substituted one or more times by a saccharide protective group; or

amino acid residue, diamino acid residue, triamino acid residue, or tetraamino acid residue, wherein the amino acid residue, diamino acid residue, triamino acid residue or tetraamino acid residue is optionally substituted one or more times by an amino acid protective group;

R 4 is methyl, ethyl, propyl, or butyl;

R 5 is methyl, ethyl, propyl, or butyl;

Z is —(C═O) n —C 0 –C 16 -alkyl-, —(C═O) n —C 0 –C 16 -alkyl-NH—, —(C═O) n —C 0 –C 16 -alkyl-O—, —(C═O) n —C 1 –C 16 -alkyl-(C═O) m —, or a covalent bond;

n is 0 or 1; and

m is 0 or 1; or

a pharmaceutically acceptable salt thereof, with at least one other active ingredient, or a pharmaceutically acceptable salt thereof, wherein the other active ingredient is selected from the group consisting of ezetimibe and carob pulp to the patient.

2. The method of claim 1 wherein the pharmaceutically effective amount of the composition of matter is provided for by the combination of a pharmaceutically effective amount or a subclinical pharmaceutically effective amount of the compound of formula I and a pharmaceutically effective amount or a subclinical pharmaceutically effective amount of the other active ingredient of the composition of matter, such that the combination results in the amount of the composition of matter being pharmaceutically effective.

3. A method for effecting the or treatment of hyperlipidemia in a patient comprising administering a pharmaceutically effective amount of a composition of matter comprising a compound of formula I

in which

R 1 is methyl, ethyl, propyl, or butyl;

R 2 is H, —OH, —NH 2 , or —NH—(C 1 –C 6 )-alkyl;

R 3 is a saccharide residue, disaccharide residue, trisaccharide residue, or tetrasaccharide residue, wherein the saccharide residue, disaccharide residue, trisaccharide residue or tetrasaccharide residue is optionally substituted one or more times by a saccharide protective group; or

amino acid residue, diamino acid residue, triamino acid residue, or tetraamino acid residue, wherein the amino acid residue, diamino acid residue, triamino acid residue or tetraamino acid residue is optionally substituted one or more times by an amino acid protective group;

R 4 is methyl, ethyl, propyl, or butyl;

R 5 is methyl, ethyl, propyl, or butyl;

Z is —(C═O) n —C 0 –C 16 -alkyl-, —(C═O) n —C 0 –C 16 -alkyl-NH—, —(C═O) n —C 0 –C 16 -alkyl-O—, —(C═O) n —C 1 –C 16 -alkyl-(C═O) m —, or a covalent bond;

n is 0 or 1; and

m is 0 or 1; or

a pharmaceutically acceptable salt thereof, with at least one other active ingredient, or a pharmaceutically acceptable salt thereof, wherein the other active ingredient is selected from ezetimibe and carob pulp to the patient.

4. The method of claim 3 wherein the pharmaceutically effective amount of the composition of matter is provided for by the combination of a pharmaceutically effective amount or a subclinical pharmaceutically effective amount of the compound of formula I and a pharmaceutically effective amount or a subclinical pharmaceutically effective amount of the other active ingredient of the composition of matter, such that the combination results in the amount of the composition of matter being pharmaceutically effective.

5. A method for effecting the or treatment of arteriosclerotic manifestations in a patient comprising administering a pharmaceutically effective amount of a composition of matter comprising a compound of formula I

in which

R 1 is methyl, ethyl, propyl, or butyl;

R 2 is H, —OH, —NH 2 , or —NH—(C 1 –C 6 )-alkyl;

R 3 is a saccharide residue, disaccharide residue, trisaccharide residue, or tetrasaccharide residue, wherein the saccharide residue, disaccharide residue, trisaccharide residue or tetrasaccharide residue is optionally substituted one or more times by a saccharide protective group; or

amino acid residue, diamino acid residue, triamino acid residue, or tetraamino acid residue, wherein the amino acid residue, diamino acid residue, triamino acid residue or tetraamino acid residue is optionally substituted one or more times by an amino acid protective group;

R 4 is methyl, ethyl, propyl, or butyl;

R 5 is methyl, ethyl, propyl, or butyl;

Z is —(C═O) n —C 0 –C 16 -alkyl-, —(C═O) n —C 0 –C 16 -alkyl-NH—, —(C═O) n —C 0 –C 16 -alkyl-O—, —(C═O) n —C 1 –C 16 -alkyl-(C═O) m —, or a covalent bond;

n is 0 or 1; and

m is 0 or 1; or

a pharmaceutically acceptable salt thereof, with at least one other active ingredient, or a pharmaceutically acceptable salt thereof, wherein the other active ingredient is selected from the group consisting of ezetimibe and carob pulp to the patient.

6. The method of claim 5 wherein the pharmaceutically effective amount of the composition of matter is provided for by the combination of a pharmaceutically effective amount or a subclinical pharmaceutically effective amount of the compound of formula I and a pharmaceutically effective amount or a subclinical pharmaceutically effective amount of the other active ingredient of the composition of matter, such that the combination results in the amount of the composition of matter being pharmaceutically effective.

7. A method for effecting the or treatment of a lipid metabolism disorder in a patient comprising administering a pharmaceutically effective amount of a composition of matter comprising a compound of formula I

in which

R 1 is methyl, ethyl, propyl, or butyl;

R 2 is H, —OH, —NH 2 , or —NH—(C 1 –C 6 )-alkyl;

R 3 is a saccharide residue, disaccharide residue, trisaccharide residue, or tetrasaccharide residue, wherein the saccharide residue, disaccharide residue, trisaccharide residue or tetrasaccharide residue is optionally substituted one or more times by a saccharide protective group; or

amino acid residue, diamino acid residue, triamino acid residue, or tetraamino acid residue, wherein the amino acid residue, diamino acid residue, triamino acid residue or tetraamino acid residue is optionally substituted one or more times by an amino acid protective group;

R 4 is methyl, ethyl, propyl, or butyl;

R 5 is methyl, ethyl, propyl, or butyl;

Z is —(C═O) n —C 0 –C 16 -alkyl-, —(C═O) n —C 0 –C 16 -alkyl-NH—, —(C═O) n —C 0 –C 16 -alkyl-O—, —(C═O) n —C 1 –C 16 -alkyl-(C═O) m —, or a covalent bond;

n is 0 or 1; and

m is 0 or 1; or

a pharmaceutically acceptable salt thereof, with at least one other active ingredient, or a pharmaceutically acceptable salt thereof, wherein the other active ingredient is selected from the group consisting of ezetimibe and carob pulp to the patient whereby the administering is effected by administering the compound of formula I and the other active ingredient of the composition of matter closely in time.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 22, 2007
From: GLOMBIK, HEINER; FRICK, WENDELIN; SCHAEFER, HANS-LUDWIG; KRAMER, WERNER
To: AVENTIS PHARMA DEUTSCHLAND GMBH
Reel/Frame 018784/0261 →
CHANGE OF NAME Recorded Nov 18, 2005
From: AVENTIS PHARMA DEUTSCHLAND GMBH
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 016793/0789 →
Priority Claims (2)
DE 101 40 169 · Aug 22, 2001 · national
DE 101 42 456 · Aug 31, 2001 · national
Continuity (2)
Continuation 1022584100 · Aug 22, 2002
Related Publication 20040097424A1 · May 20, 2004