A Study to Assess the Levels in Blood Plasma of BMS-986278 in Healthy Participants Following Administration of Tablets, With or Without Food, and in the Presence of an Antacid (Esomeprazole)
Completed · Phase 1
Conditions studied: Healthy Participants
In brief
The purpose of this study is to assess levels in blood plasma of BMS-986278 and the food effect in healthy participants.
Key facts
- Study ID
- NCT04468815
- Run by
- Bristol-Myers Squibb
- People needed
- 24
- Starts
- 2020-07-10
- Expected to finish
- 2020-10-07
- Last updated by the study team
- 2022-05-10
Who can join
Age: 21 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy participants, as determined by no clinically significant deviation from normal in medical history, physical examination, ECGs, and clinical laboratory determinations in the opinion of the investigator
- Women and men must agree to follow specific methods of contraception
You may not qualify if…
- Women of childbearing potential (WOCBP) and Women who are pregnant or breastfeeding
- Any significant acute or chronic medical condition that presents a potential risk to the participant and/or that may compromise the objectives of the study
- Exposure to any investigational drug or placebo within 4 weeks of first study treatment administration.
- History of any significant drug and/or food allergies (such as anaphylaxis or hepatotoxicity)
- Other protocol-defined inclusion/exclusion criteria apply
Where it is running
- ICON (LPRA) - Salt Lake — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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