Coronary Artery Disease Clinical Trial
Official title:
A Randomized, Open-label, Single-dose, Two-sequence, Two-period Crossover Study to Investigate The Pharmacokinetics Between a Tablet Containing 75 mg of Clopidogrel and 100 mg of Aspirin and The Simultaneous Administration of The Separate Formulations of The Two Drugs in Healthy Male Volunteers
This is a randomized, open-label, single-dose, two-sequence, two-period crossover study to investigate the pharmacokinetics between a tablet containing 75 mg of Clopidogrel and 100 mg of Aspirin and the simultaneous administration of the separate formulations of the two drugs in healthy male volunteers.
Eligibility for participation of this study will be determined from demographic information,
medical history, physical examination, electrocardiogram (ECG) and clinical laboratory tests
within 4 weeks before study drug administration. Subjects suitable for this study will be
admitted to the Clinical Trial Center of Ajou Medical Center on the day before dosing, and
they will overnight-fasted from 10 p.m. of Day -1.
Subjects will be dosed study drug (a tablet containing 75 mg of Clopidogrel and 100 mg of
Aspirin, or the simultaneous administration of the separate formulations of the two drugs)
orally with 240 mL of water around 8 a.m. of Day 1. Subjects will be performed scheduled
pharmacokinetic sampling upto 24 hours.
After 2 weeks of washout period, Subjects will be dosed study drug by crossover manner, and
will be performed scheduled pharmacokinetic sampling upto 24 hours.
Study participation will be ended on post-study visit (Day 25).
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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