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A Randomized, Double-Blind, Placebo-controlled, Single Continuous Intravenous Infusion Study of BMS-986231 to Assess Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics in Healthy Japanese and Non- Asian Participants
The purpose of this Phase 1 study is to evaluate the safety, tolerability, PK, and pharmacodynamics (PD) of BMS-986231 in healthy Japanese and Non-Asian participants. There is no formal hypothesis to be statistically tested.
Age
18 - 40 years
Sex
ALL
Healthy Volunteers
Yes
West Coast Clinical Trials, Llc
Cypress, California, United States
Start Date
October 4, 2016
Primary Completion Date
May 26, 2017
Completion Date
May 26, 2017
Last Updated
May 31, 2017
56
ACTUAL participants
BMS-986231
DRUG
BMS-986231 Placebo
DRUG
Lead Sponsor
Bristol-Myers Squibb
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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