Abstract
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▴ Lamifiban is an intravenously administered, selective, reversible, nonpeptide glycoprotein IIb/IIIa receptor antagonist which inhibits platelet aggregation and thrombus formation by preventing the binding of fibrinogen to platelets.
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▴ In trials in patients with non-Q wave myocardial infarction (MI) or unstable angina pectoris (PARAGON A and the Canadian Lamifiban Study), the incidence of clinical events at 30 days in patients receiving lamifiban (1 to 5 µg/min) was not significantly different from that in patients receiving aspirin plus heparin or aspirin alone.
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▴ In PARAGON A, the incidence of clinical events at 6 months was significantly lower after lamifiban (with or without heparin) and aspirin therapy than after standard heparin and aspirin therapy.
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▴ A large phase III trial (PARAGON B) is under way comparing lamifiban plus aspirin and heparin with standard aspirin and heparin therapy in patients with non-Q wave MI or unstable angina pectoris.
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▴ In clinical trials, the most common adverse events associated with lamifiban were bleeding complications which were increased by the concomitant administration of heparin.
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Dooley, M., Goa, K.L. Lamifiban. Drugs 57, 215–221 (1999). https://doi.org/10.2165/00003495-199957020-00009
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DOI: https://doi.org/10.2165/00003495-199957020-00009