US2016106800A1PendingUtilityA1
Methods for the prevention or treatment of heart failure
Est. expiryOct 5, 2029(~3.2 yrs left)· nominal 20-yr term from priority
C07K 5/1016A61K 38/07A61P 9/00A61K 45/06C07K 5/0817C07K 5/1019A61K 9/0019
54
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Claims
Abstract
The disclosure provides methods of preventing or treating heart failure in a mammalian subject. The methods comprise administering to the subject an effective amount of an aromatic-cationic peptide to subjects in need thereof.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating heart failure or hypertensive cardiomyopathy in a mammalian subject, comprising administering to the mammalian subject in need thereof a therapeutically effective amount of the peptide D-Arg-2′6′-Dmt-Lys-Phe-NH 2 or Phe- D -Arg-Phe-Lys-NH 2 .
2 . The method of claim 1 , wherein the peptide is D-Arg-2′6′-Dmt-Lys-Phe-NH 2 .
3 . The method of claim 1 , wherein the peptide is Phe- D -Arg-Phe-Lys-NH 2 .
4 . The method of claim 1 , wherein the subject is suffering from heart failure.
5 . The method of claim 4 , wherein the heart failure results from hypertension; ischemic heart disease; exposure to a cardiotoxic compound; myocarditis; thyroid disease; viral infection; gingivitis; drug abuse; alcohol abuse; pericarditis; atherosclerosis; vascular disease; hypertrophic cardiomyopathy; acute myocardial infarction; left ventricular systolic dysfunction; coronary bypass surgery; starvation; an eating disorder; or a genetic defect.
6 . The method of claim 1 , wherein the subject is suffering hypertensive cardiomyopathy.
7 . The method of claim 1 , wherein myocardial contractility and cardiac output in the subject administered the peptide are increased compared to a control subject not administered the peptide.
8 . The method of claim 7 , wherein the myocardial contractility and cardiac output in the subject are increased at least 10% compared to a control subject not administered the peptide.
9 . The method of claim 1 , wherein the subject is a human.
10 . The method of claim 1 , wherein the peptide is administered orally, topically, systemically, intravenously, subcutaneously, intraperitoneally, or intramuscularly.
11 . The method of claim 1 , further comprising separately, sequentially or simultaneously administering a cardiovascular agent to the subject.
12 . The method of claim 11 , wherein the cardiovascular agent is selected from the group consisting of: an anti-arrhthymia agent, a vasodilator, an anti-anginal agent, a corticosteroid, a cardioglycoside, a diuretic, a sedative, an angiotensin converting enzyme (ACE) inhibitor, an angiotensin II antagonist, a thrombolytic agent, a calcium channel blocker, a throboxane receptor antagonist, a radical scavenger, an anti-platelet drug, a β-adrenaline receptor blocking drug, α-receptor blocking drug, a sympathetic nerve inhibitor, a digitalis formulation, an inotrope, and an antihyperlipidemic drug.
13 . A method for increasing myocardial contractility and cardiac output in a subject suffering from heart failure or hypertensive cardiomyopathy comprising administering to the subject a therapeutically effective amount of the peptide D-Arg-2′6′-Dmt-Lys-Phe-NH 2 or Phe- D -Arg-Phe-Lys-NH 2 .Cited by (0)
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