Therapeutic dosing of a neuregulin or a subsequence thereof for treatment or prophylaxis of heart failure
View Patent ↗The invention relates to treatment of heart failure in a mammal. Accordingly, the invention is directed to establishing a dosing regimen whereby the therapeutic benefits conferred by administration of a neuregulin such as glial growth factor 2 (GGF2) or a subsequence thereof are maintained and/or enhanced, while concomitantly minimizing any potential side effects.
1. A method of reducing side effects due to supraphysiological levels of a peptide comprising an epidermal growth factor-like (EGF-like) domain of glial growth factor 2 (GGF2) upon administration while treating or preventing heart failure in a mammal over a prolonged duration, said method comprising:
administering a therapeutically effective amount of said peptide to said mammal at an interval of at least 96 hours, wherein said therapeutically effective amount is effective to reduce side effects due to supraphysiological levels of said peptide while treating or preventing heart failure in said mammal.
2. The method according to claim 1 , wherein said side effects are nerve sheath hyperplasia, mammary hyperplasia, renal nephropathy, hypospermia, hepatic enzyme elevation, heart valve changes, or skin changes.
3. The method according to claim 1 , wherein said peptide administered at an interval of at least 96 hours elicits fluctuations in the serum levels of said peptide.
4. The method according to claim 1 , wherein said peptide administered at an interval of at least 96 hours does not maintain steady state therapeutic levels of said peptide in the serum of said subject.
5. The method according to claim 1 , wherein said subject is exposed to a cardiotoxic agent.
6. The method according to claim 5 , wherein said cardiotoxic agent is cocaine, alcohol, an anti-ErbB2 antibody, an anti-HER2 antibody, and/or an anthracycline antibiotic.
7. The method according to claim 6 , wherein said subject is exposed to said anti-ErbB2 or said anti-HER2 antibody during or after anthracycline antibiotic exposure.
8. The method according to claim 5 , wherein said peptide is administered prior to exposure to said cardiotoxic agent.
9. The method according to claim 5 , wherein said peptide is administered after exposure to said cardiotoxic agent.
10. The method according to claim 1 , wherein said subject is suffering from myocarditis, thyroid disease, viral infection, gingivitis, drug abuse, alcohol abuse, periocarditis, atherosclerosis, vascular disease, hypertrophic cardiomyopathy, acute myocardial infarction, previous myocardial infarction, left ventricular systolic dysfunction, coronary bypass surgery, starvation, radiation exposure, an eating disorder, and/or a genetic defect.
11. The method according to claim 1 , wherein said peptide is a recombinant human GGF2 or a fragment thereof.
12. The method according to claim 1 , wherein said peptide comprises a polypeptide sequence:
(SEQ ID NO: 4)
SHLVKCAEKEKTFCVNGGECFMVKDLSNPSRYLCKCPNEFTGDRCQNYV
MASFYSTSTPFLSLPE.