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RECRUITING
NCT07283263
PHASE1

A Study to Evaluate the Safety, Tolerability, and Drug Levels of BMS-986521 in Healthy Participants.

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

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

Interventions

DRUG

BMS-985521

Specified dose on specified days.

OTHER

Placebo

Specified dose on specified days

Locations (1)

CenExel ACT (Formerly Anaheim Clinical Trials; LLC)

Anaheim, California, United States