Peripheral Artery Disease Clinical Trial
Official title:
A Randomized, Open Label, Multiple Does, Crossover Study to Compare the Safety/Tolerability and Pharmacokinetics Between Pleetal SR Cap. and Cilostan CR Tab. in Healthy Volunteers
This is a randomized, open-label, multiple-dose, two-sequence, two-period crossover study to to compare the safety/tolerability and pharmacokinetics between Pletaal SR Cap. and Cilostan CR Tab. in healthy 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 CHA Bundang Medical Center on the day before dosing
(Day -1).
From Day 1 to 5, Subjects will be dosed study drug (Pletaal SR Cap. 200 mg once a day or
Cilostan CR Tab. 200mg once a day).
Pharmacokinetic samplings will be done upto 24 hours after 1st study drug dosing and upto 72
hours after 5th study drug dosing.
After 9 days of washout period (Day 15), Subjects will be dosed study drug and
pharmacokinetic samplings will be done by crossover manner.
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