IP Library Granted Patent US 8,809,358
Granted Patent B2
US 8,809,358 · App. 12/266,018 · Granted Aug 19, 2014

Use of IκB-kinase inhibitors in pain therapy

Inventors: Martin Michaelis (Frankfurt am Main, DE); Olaf Ritzeler (Frankfurt am Main, DE); Gerhard Jaehne (Frankfurt am Main, DE); Karl Rudolphi (Frankfurt am Main, DE); Gerd Geisslinger (Frankfurt am Main, DE); Hans-Georg Schaible (Frankfurt am Main, DE)
Assignee: Sanofi-Aventis Deutschland GmbH
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Quick Facts
Patent No.
US 8,809,358
App. No.
12/266,018
Granted
Aug 19, 2014
Kind
B2
Abstract

The present invention relates to the use of IκB-kinase Inhibitors and methods for the prophylaxis and therapy for treating pain comprising administering such compounds.

Claims (17)

1. A method for treating pain of an inflammatory etiology in a patient in need thereof, the method comprising administering to the patient a pharmaceutically effective amount of an IκB-kinase inhibitor of a compound of formula Ia:

or a stereoisomeric form thereof or a mixture of stereoisomeric forms in any ratio, or a physiologically tolerated salt thereof, wherein,

E is N or CH;

M is N or CH;

R21 is a group selected from hydrogen atom, F, Cl, I, and Br;

R31 is a hydrogen atom;

R22 is a heteroaryl radical selected from:

5-oxo-4,5-dihydro-[1,3,4]oxadiazole;

triazole;

—C(O)—OR 15 , wherein R 15 is hydrogen atom or —(C 1 -C 4 )-alkyl; and

—C(O)—N(R 17 )—R 18 , wherein R 17 and R 18 are, independently of each other, selected from hydrogen atom, —(C 1 -C 4 )-alkyl-OH, —O—(C 1 -C 4 )-alkyl, and —(C 1 -C 4 )-alkyl;

R23 is a hydrogen atom or —(C 1 -C 4 )-alkyl; and

R24 is a heteroaryl radical selected from thiazole, pyridine, and pyrimidine, wherein the heteroaryl radical is unsubstituted, or substituted, one, two or three times, independently of each other, by groups selected from F, Cl, Br, I, —(C 1 -C 5 )-alkyl, and trifluoromethyl; or

R24 is a phenyl radical, wherein the phenyl radical is unsubstituted, or substituted, one, two or three times, independently of each other, by groups selected from F, Cl, Br, I, —(C 1 -C 5 )-alkyl, and trifluoromethyl.

2. The method according to claim 1 wherein the pain is chronic pain.

3. The method according to claim 2 wherein the chronic pain is selected from: pain associated with chronic musculoskeletal diseases, pain associated with osteoarthritis or rheumatoid arthritis, pain associated with intestinal inflammation, pain associated with cardiac muscle inflammation, pain associated with multiple sclerosis, and pain associated with neuritis.

4. The method according to claim 2 , wherein the chronic pain is associated with chronic musculoskeletal diseases, osteoarthritis, or rheumatoid arthritis.

Assignments (2)
CHANGE OF NAME Recorded Jul 9, 2014
From: AVENTIS PHARMA DEUTSCHLAND GMBH
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 033283/0765 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 19, 2012
From: MULLER, GUNTER, DR.; DLUGAI, SILKE, DR.; VOSS, DORTHE, DR.; BOLES, ECKHARD, DR.
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 028071/0156 →
Priority Claims (1)
DE 102 37 723 · Aug 17, 2002 · national
Continuity (3)
Continuation 10642974 · Aug 18, 2003
Provisional Application 60434628 · Dec 19, 2002
Related Publication 20090069358A1 · Mar 12, 2009