Local Institution
Yokohama, Kanagawa, 2320064, Japan
NCT Number: NCT00828646
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
Looking for future studies?
Notify Me20 year and older
All sexes
Interventional
Phase 1
Yokohama, Kanagawa, 2320064, Japan
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Capsules, Oral, 50 mg, once daily, 14 days
Capsules, Oral, once daily, 14 days
Time frame: Within 30 days after the follow-up evaluation on Day 28
Time frame: Day 21
Bristol-Myers Squibb
Industry
Placebo-Controlled, Ascending Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-708163 in Healthy Male Japanese Subjects and a Comparison to Healthy Elderly Japanese Subjects
Acronym: JMAD
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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