Effects of ticlopidine, a new platelet aggregation inhibitor in man

Clinical Pharmacology and Therapeutics - Tập 18 Số 4 - Trang 485-490 - 1975
J.J. Thebault1, Charles E. Blatrix1, J Blanchard1, E Panak1
1Centre Hospitalier Intercommunal de Créteil, and Departement Recherche et Développement Parcor

Tóm tắt

Ticlopidine is a new platelet aggregation inhibitor. The effect of this drug was studied on 55 subjects, healthy volunteers and hospitalized patients. The action requires 24 to 48 hr to appear, and lasts more than 3 days. A dose‐effect relationship was studied with oral daily doses ranging from 250 to 1,000 mg during 1 wk; it showed a 50% inhibition on adenosine diphosphate (ADP )‐induced aggregation at 2 μM concentration on an oral daily dose of 450 mg. No action was found on collagen‐induced aggregation, and a mild effect was observed on platelet adhesiveness. Clinical tolerance was assessed in patients given ticlopidine in oral doses up to 500 mg /day during several weeks, showing no overt side effects and no change in the safety parameters.

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