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Randomized, Double-Blinded, Placebo-Controlled, Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-708163 125 mg in Healthy Japanese and Non-Japanese Subjects
The purpose of this study is to assess the safety and tolerability of multiple oral daily doses of BMS-708163 in healthy young male subjects
Age
20 - 45 years
Sex
MALE
Healthy Volunteers
Yes
California Clinical Trials Medical Group
Glendale, California, United States
Start Date
March 1, 2010
Primary Completion Date
June 1, 2010
Completion Date
June 1, 2010
Last Updated
January 25, 2011
22
ACTUAL participants
BMS-708163
DRUG
Placebo
DRUG
Lead Sponsor
Bristol-Myers Squibb
NCT07178210
NCT04123314
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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