IP Library Granted Patent US 8,106,099
Granted Patent B2
US 8,106,099 · App. 10/796,894 · Granted Jan 31, 2012

Combination of phenylcarboxamides with blockers of the IKr channel and their use for the treatment of atrial arrhythmias

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Quick Facts
Patent No.
US 8,106,099
App. No.
10/796,894
Granted
Jan 31, 2012
Kind
B2
Abstract

The invention relates to the combination of one or more IK r channel blockers and of one or more Kv1.5 blockers, in particular phenyl-carboxamides of the formula Ia or Ib or pharmaceutically tolerable salts thereof, and the use of the combination for the treatment of atrial arrhythmias.

Claims (12)

1. A pharmaceutical preparation for treating atrial arrhythmia in a mammal, said preparation comprising a combination of:

2′-{[2-(4-methoxyphenyl)acetylamino]methyl}biphenyl-2-carboxylic acid (2-pyridin-3-ylethyl)amide and ibutilide in a weight ratio of 10,000:1 to 1:1; or

or the physiologically tolerable salts thereof,

and a pharmaceutically innocuous solvent, wherein the preparation provides an hourly dose of 3 mg per kg of said 2′-{[2-(4-methoxyphenyl)acetylamino]methyl}biphenyl-2-carboxylic acid (2-pyridin-3-ylethyl)amide when administered to said mammal.

2. The pharmaceutical preparation of claim 1 wherein the preparation provides an hourly dose of 0.12 mg per kg of said ibutilide when administered to said mammal.

3. The pharmaceutical preparation of claim 1 , wherein said weight ratio is 100:1 to 5:1.

4. A pharmaceutical preparation for treating atrial arrhythmia in a mammal, said preparation comprising a combination of:

2′-{[2-(4-methoxyphenyl)acetylamino]methyl}biphenyl-2-carboxylic acid (2-pyridin-3-ylethyl)amide and dofetilide in a weight ratio of 10,000:1 to 1:1; or

or the physiologically tolerable salts thereof,

and a pharmaceutically innocuous solvent, wherein the preparation provides an hourly dose of 3 mg per kg of said 2′-{[2-(4-methoxyphenyl)acetylamino]methyl}biphenyl-2-carboxylic acid (2-pyridin-3-ylethyl)amide when administered to said mammal.

5. The pharmaceutical preparation of claim 4 wherein the preparation provides an hourly dose of 0.12 mg per kg of said dofetilide when administered to said mammal.

6. The pharmaceutical preparation of claim 4 , wherein said weight ratio is 100:1 to 5:1.

Assignments (2)
CHANGE OF NAME Recorded Nov 18, 2005
From: AVENTIS PHARMA DEUTSCHLAND GMBH
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 016793/0789 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2004
From: BRENDEL, DR. JOACHIM; WIRTH, DR. KLAUS; GOEGELEIN, DR. HEINZ; ALLESSIE, PROF MAURITS; BLAAUW, DR. YURI
To: AVENTIS PHARMA DEUTSCHLAND GMBH
Reel/Frame 015369/0291 →