The purpose of this study is to evaluate the safety profile, tolerability, pharmacokinetics, and pharmacodynamics following 14-day multiple oral doses BMS-708163 in healthy young male Japanese and healthy elderly male and female Japanese subjects
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
32
Capsules, Oral, 50 mg, once daily, 14 days
Capsules, Oral, 100 mg/day, once daily, 14 days
Capsules, Oral, 75 or 100 mg/day, once daily, 14 days
Local Institution
Yokohama, Kanagawa, Japan
Adverse Events
Time frame: Within 30 days after the follow-up evaluation on Day 28
Plasma concentration
Time frame: Day 21
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Capsules, Oral, once daily, 14 days