Claims for Patent: 7,226,907

Summary for Patent: 7,226,907

Title:	Cardiac muscle function and manipulation
Abstract:	A method of causing cardiomyocyte growth and/or differentiation, the method comprising exposing a cardiomyocyte to neuregulin (NRG) thereby activating the MAP kinase pathway in the cardiomyocyte and causing growth and/or differentiation of the cardiomyocyte. Use of neuregulin, neuregulin polypeptide, neuregulin derivatives, or compounds which mimic the activities of neuregulins in the treatment or management of heart disease and heart failure in a mammal.
Inventor(s):	Zhou; Mingdong (La Jolla, CA)
Assignee:	Zensun (Shanghai) Science & Technology Limited (Shanghai, CN)
Application Number:	09/980,672
Patent Claims:	1. A method of inducing remodeling of cardiac muscle cell sarcomeric and cytoskeleton structures or cell-cell adhesions, which method comprises contacting cardiac muscle cells with a neuregulin protein consisting of the amino acid sequence set forth in SEQ ID NO:2, in the amount sufficient to activate the MAP kinase pathway in said cardiac muscle cells and induce remodeling of said cardiac muscle cell sarcomeric and cytoskeleton structures or cell-cell adhesions. 2. The method of claim 1, wherein the neuregulin protein is used in an amount that is at least 10.sup.-8M. 3. The method of claim 1, wherein the cardiomyocyte or the cardiac muscle cells exist in a mammal. 4. The method of claim 3, wherein the mammal is a human. 5. The method of claim 4, wherein the human has or is suspected of having a heart failure. 6. The method of claim 5, wherein the heart failure is a disease state selected from the group consisting of congestive heart failure, myocardial infarction, tachyarrhythmia, familial hypertrophic cardiomyopathy, ischaemic heart disease, idiopathic dilated cardiomyopathy and myocarditis. 7. The method of claim 5, wherein the heart failure is in the form of ischaemic, congenital, rheumatic, or idiopathic. 8. The method of claim 5, wherein the heart failure results from disassociation of cardiac muscle cell-cell adhesion and/or the disarray of sarcomeric structures in the mammal. 9. The method of claim 3, wherein the neuregulin protein is administered with a pharmaceutically acceptable carrier or excipient. 10. The method of claim 1, wherein the contact of the cardiac muscle cells with the neuregulin protein decreases DNA synthesis in the cardiac muscle cells. 11. The method of claim 1, wherein the contact of the cardiac muscle cells with the neuregulin protein results in sustained activation of the MAP kinase pathway in the cardiac muscle cells. 12. The method of claim 3, wherein the neuregulin protein is administered orally, using a sustained-release system or via injection or infusion. 13. The method of claim 12, wherein the injection or infusion is selected from the group consisting of intravenous, intraperitoneal, intracerebral, intramuscular, intraocular, intraarterial and intralesional injection or infusion. 14. The method of claim 1, which further comprises contacting the cardiac muscle cells with an effective amount of an agent which causes cardiac hypertrophy or congestive heart failure. 15. The method of claim 14, wherein the agent which causes cardiac hypertrophy or congestive heart failure is fludrocortisone acetate or herceptin. 16. The method of claim 1, which further comprises contacting the cardiac muscle cells with an effective amount of an agent that acts to suppress a hypertrophy induction pathway different from the pathway suppressed by the neuregulin. 17. The method of claim 16, wherein the agent that acts to suppress a hypertrophy induction pathway different from the pathway suppressed by the neuregulin is selected from the group consisting of a cardiotrophic inhibitor, an angiotensin-converting enzyme (ACE) inhibitor, a human growth hormone, an IGF-I, an anti-hypertrophic, myocardiotrophic factor, an anti-arrhythmic factor and an inotropic factor. 18. The method of claim 1, which further comprises contacting the cardiac muscle cells with an effective amount of an angiotensin-converting enzyme (ACE) inhibitor. 19. The method of claim 18, wherein the ACE inhibitor is selected from the group consisting of quinapril, ramipril, captopril, benazepril, fosinopril, lisinopril, enalapril and lisinopril. 20. The method of claim 1, which further comprises contacting the cardiac muscle cells with an effective amount of an agent for treating hypertension. 21. The method of claim 20, wherein the agent for treating hypertension is selected from the group consisting of an antibody to the endothelin receptor, a .beta.-adrenoreceptor antagonist, an .alpha..sub.1-noreceptor antagonist, an anti-oxidant, a .beta.-blocker and a growth hormone. 22. A method for treating or delaying disassociation of cardiac muscle cell-cell adhesion and/or the disarray of sarcomeric structures in a mammal, which method comprises administering to a mammal, to which such treatment or delay is needed or desirable, a neuregulin protein consisting of the amino acid sequence set forth in SEQ ID NO:2, in an amount sufficient to activate the MAP kinase pathway in said mammal, whereby said disassociation of cardiac muscle cell-cell adhesion and/or the disarray of sarcomeric structures is treated or delayed in said mammal. 23. The method of claim 22, wherein the mammal is a human. 24. The method of claim 23, wherein the human has or is suspected of having a heart failure. 25. The method of claim 24, wherein the heart failure is a disease state selected from the group consisting of congestive heart failure, myocardial infarction, tachyarrhythmia, familial hypertrophic cardiomyopathy, ischaemic heart disease, idiopathic dilated cardiomyopathy and myocarditis. 26. The method of claim 24, wherein the heart failure is in the form of ischaemic, congenital, rheumatic, or idiopathic. 27. The method of claim 22, wherein administration of the neuregulin protein decreases DNA synthesis in the cardiac muscle cells of the mammal. 28. The method of claim 22, wherein administration of the neuregulin protein results in sustained activation of the MAP kinase pathway in the cardiac muscle cells of the mammal.

Details for Patent 7,226,907

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	09/25/1998		2018-12-21
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	02/10/2017		2018-12-21