IP Library Granted Patent US 6,894,024
Granted Patent B2
US 6,894,024 · App. 09/982,978 · Granted May 17, 2005

Treatment of hibernating myocardium and diabetic cardiomyopathy with a GLP-1 peptide

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,894,024
App. No.
09/982,978
Granted
May 17, 2005
Kind
B2
Abstract

Hibernating myocardium is characterized by viable myocardium with impaired function due to localized reduced perfusion. Hibernating myocytes retain cellular integrity, but cannot sustain high-energy requirements of contraction. High plasma levels of catecholamines, such as norepinepherine, are believed to be predictive of mortality from hibernating myocardium. Likewise, high levels of catecholamines lead to cardiomyopathy in patients with diabetes. GLP-1 reduces plasma norepinepherine levels, and it thus is useful in a method of treating hibernating myocardium or diabetic cardiomyopathy.

Claims (9)

1. A method of treating a patient suffering from diabetic cardiomyopathy, comprising administering an effective amount of compound selected from the group consisting of Glucagon-Like Peptide-1 (GLP-1), GLP-1 analogs, and GLP-1-like peptides, to a patient suffering from diabetic cardiomyopathy.

2. The method of claim 1 , wherein the administration is continuous.

3. The method of claim 1 , wherein the administration is parenteral.

4. The method of claim 1 , wherein said effective amount of said compound is effective to cause a reduction in the plasma or heart norepinepherine level.

5. The method of claim 3 , wherein said compound is administered in a dose of from about 0.1-10 pmol/kg/min.

6. The method of claim 1 wherein said compound is administered subcutaneously in a dose of about 0.5-50 pmol/kg/min.

7. The method of claim 1 wherein said compound is administered in a dose of up to 10.0 nmol/kg.

8. The method of claim 1 , wherein said compound is administered intravenously in a dose of about 0.1-10 pmol/kg/min.

9. The method of claim 1 , wherein said compound is selected from the group consisting of GLP-1(1-37), GLP-1(1-36)NH 2 , GLP-1(7-37), and GLP-1(7-36)NH2.

Assignments (5)
AMYLIN PHARMACEUTICALS, LLC ASSIGNS AN EQUAL AND UNDIVIDED ONE-HALF OF ITS ENTIRE RIGHT, TITLE AND INTEREST TO ASTRAZENECA PHARMACEUTICALS LP Recorded Oct 26, 2012
From: AMYLIN PHARMACEUTICALS, LLC
To: ASTRAZENECA PHARMACEUTICALS LP
Reel/Frame 029195/0555 →
CHANGE OF NAME Recorded Oct 25, 2012
From: AMYLIN PHARMACEUTICALS, INC.
To: AMYLIN PHARMACEUTICALS, LLC
Reel/Frame 029198/0340 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2003
From: BIONEBRASKA, INC. A/K/A RESTORAGEN, INC.
To: AMYLIN PHARMACEUTICALS, INC.
Reel/Frame 013729/0401 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2002
From: COOLIDGE, THOMAS R.; EHLERS, MARIO
To: BIONEBRASKA, INC.
Reel/Frame 012470/0642 →
SECURITY INTEREST Recorded Dec 18, 2001
From: RESTORAGEN, INC., F/K/A BIONEBRASKA, INC.
To: MEDTRONIC INTERNATIONAL, LTD.
Reel/Frame 012350/0779 →