IP Library Granted Patent US 8,076,283
Granted Patent B2
US 8,076,283 · App. 12/655,361 · Granted Dec 13, 2011

Methods for treating congestive heart failure

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Quick Facts
Patent No.
US 8,076,283
App. No.
12/655,361
Granted
Dec 13, 2011
Kind
B2
Abstract

The invention features methods of treating or preventing congestive heart failure by administering a polypeptide containing an epidermal growth factor-like domain encoded by a neuregulin gene.

Claims (18)

1. method for treating congestive heart failure in a mammal, said method comprising administering an NRG-3 polypeptide comprising an epidermal growth factor-like (EGF-like) domain in an amount effective to treat congestive heart failure in said mammal.

2. The method of claim 1 , wherein said polypeptide is encoded by the NRG-3 gene.

3. he method of claim 1 , wherein said mammal is a human.

4. The method of claim 1 , wherein said congestive heart failure results from hypertension; ischemic heart disease; exposure to a cardiotoxic compound; myocarditis; thyroid disease; viral infection; gingivitis; drug abuse; alcohol abuse; periocarditis; atherosclerosis; vascular disease; hypertrophic cardiomyopathy; acute myocardial infarction; left ventricular systolic dysfunction; coronary bypass surgery; starvation; an eating disorder; or a genetic defect.

5. The method of claim 4 , wherein said mammal has undergone a myocardial infarction.

6. The method of claim 4 , wherein said cardiotoxic compound is an anthracycline; alcohol; or cocaine.

7. The method of claim 6 , wherein said anthracyline is doxorubicin, or daunomycin.

8. The method of claim 7 , wherein an anti-ErbB2 or anti-HER2 antibody is administered to said mammal before, during, or after anthracycline administration.

9. The method of claim 4 , wherein said cardiotoxic compound is an anti-ErbB2 or anti-HER2 antibody.

10. The method of claim 4 , wherein said polypeptide is administered prior to exposure to said cardiotoxic compound.

11. The method of claim 4 , wherein said polypeptide is administered during exposure to said cardiotoxic compound.

12. The method of claim 4 , wherein said polypeptide is administered after exposure to said cardiotoxic compound.

13. The method of claim 1 , wherein said polypeptide is administered prior to the diagnosis of congestive heart failure in said mammal.

14. The method of claim 1 , wherein said polypeptide is administered after the diagnosis of congestive heart failure in said mammal.

15. The method of claim 1 , wherein said polypeptide is administered to a mammal that has undergone compensatory cardiac hypertrophy.

16. The method of claim 1 , wherein administration of said polypeptide maintains left ventricular hypertrophy.

17. The method of claim 1 , wherein said method prevents progression of myocardial thinning.

18. The method of claim 1 , wherein administration of said polypeptide inhibits cardiomyocyte apoptosis.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded May 31, 2017
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: NEURONEX, INC.; CIVITAS THERAPEUTICS, INC.; ACORDA THERAPEUTICS, INC.
Reel/Frame 042643/0878 →
SECURITY INTEREST Recorded Jun 10, 2016
From: ACORDA THERAPEUTICS, INC.; CIVITAS THERAPEUTICS, INC.; NEURONEX, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 038950/0436 →