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Single and Multiple Dose Study to Evaluate Safety and Pharmacokinetics of BMS-986533 in Healthy Participants and Assessments of Food and pH Effects on Relative Bioavailability, and Drug-Drug Interaction Potential in Healthy Participants
Sponsor: Bristol-Myers Squibb
Summary
The purpose of this study is to evaluate the safety and pharmacokinetics of BMS-986533 in healthy participants receiving single and multiple doses, to assess food and pH effects on the relative bioavailability of BMS-986533, and the P-gp and BCRP-mediated drug-drug interaction potential of the study drug
Official title: A Phase 1, Randomized, Double-blind, Placebo-controlled, First-in-Human, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986533 in Healthy Participants, an Open-label Assessment of Food and pH Effects on the Relative Bioavailability of BMS-986533, and an Open-label Study to Evaluate P-gp- and BCRP-mediated Drug-Drug Interaction Potential of BMS-986533 in Healthy Participants
Key Details
Gender
All
Age Range
18 Years - 55 Years
Study Type
INTERVENTIONAL
Enrollment
118
Start Date
2026-06-30
Completion Date
2027-06-01
Last Updated
2026-06-05
Healthy Volunteers
Yes
Conditions
Interventions
BMS-986533
Specified dose on specified days
Famotidine
Specified dose on specified days
Placebo
Specified dose on specified days
Dabigatran Etexilate
Specified dose on specified days
Rosuvastatin
Specified dose on specified days
Locations (1)
Local Institution - 0001
Lincoln, Nebraska, United States