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A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-986521 in Healthy Participants.
Sponsor: Bristol-Myers Squibb
Summary
The purpose of this study is to evaluate the safety, tolerability, and drug levels of BMS-986521 following single and multiple ascending doses of BMS-986521 in healthy adult participants, and to evaluate potential food effects on BMS-986521 exposure.
Official title: A Phase 1, Randomized, Placebo-Controlled, Double-Blind, First-in-Human Study Evaluating Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of Orally Administered BMS-986521 in Healthy Adult Participants
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
INTERVENTIONAL
Enrollment
106
Start Date
2025-12-23
Completion Date
2026-11-17
Last Updated
2026-01-07
Healthy Volunteers
Yes
Conditions
Interventions
BMS-985521
Specified dose on specified days.
Placebo
Specified dose on specified days
Locations (1)
CenExel ACT (Formerly Anaheim Clinical Trials; LLC)
Anaheim, California, United States