Use of moxonidine for postmyocardial infarction treatment

Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form

Reexamination Certificate

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C424S422000, C424S464000, C514S821000, C514S256000, C514S269000, C514S393000, C514S398000, C514S399000

Reexamination Certificate

active

07041303

ABSTRACT:
A method of treating myocardial damage secondary to myocardial infarction using moxonidine or a physiologically compatible salt thereof. Pharmaceutical preparations containing moxonidine and its physiologically compatible acid addition salts are suitable for use in acute myocardial infarction and/or postmyocardial infarction management. In addition to a beneficial influence, promoting recovery and/or rehabilitation, on the myocardial status following myocardial infarction, moxonidine and its physiologically compatible acid addition salts, especially when used in the management of postmyocardial infarction patients in the chronic stage, also show a preventive effect against the progression of heart failure after myocardial infarction.

REFERENCES:
patent: 0317855 (1990-08-01), None
patent: WO9746241 (1997-12-01), None
Howes et al. Comparative effects of angiotensin converting enzyme inhibition (perindopril) or diuretic therapy on cardiac hypertrophy and sympathetic activity following myocardial infarction in rats. Cardiovascular Drug Therapy, Feb., 1991, 5(1):147-152.
Rene Roland Wenzel, “I1-Imidazoline Agonist Moxonidine Decrease Sympathetic Nerve Activity and Blood Pressure in Hypertensives” Hypertension, Dec. 1998.
W. Lada, “Imidazoline-prefering receptors and the I1-imidazoline blocking therapy” Pol. Merk. Lek., 1996.
Istvan Lepran, “Effect of Moxonidine on Arrhythmias Induced by Coronary Artery Occlusion and Reperfusion” Journal of Cardiovascular Pharmacology, 1994.

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