Study to Evaluate the Safety, Pharmacokinetics and Target Engagement of BMS-986142 in Healthy Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Healthy Adult
In brief
The purpose of this study is to evaluate the safety, pharmacokinetics, and target engagement of BMS-986142 in healthy subjects.
Key facts
- Study ID
- NCT02257151
- Run by
- Bristol-Myers Squibb
- People needed
- 118
- Starts
- 2014-09-01
- Expected to finish
- 2015-08-01
- Last updated by the study team
- 2015-09-24
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male and female subjects as determined by no clinically significant deviation from normal in medical history, physical examination, ECGs, and clinical laboratory determinations
- Body Mass Index (BMI) of 18 to 32 kg/m2, inclusive. BMI=weight (kg)/[height(m)]2
You may not qualify if…
- Any significant acute or chronic medical illness
- Current or recent (within 3 months of study drug administration) gastrointestinal disease
- Any major surgery within 4 weeks of study drug administration
- Any gastrointestinal surgery that could impact upon the absorption of study drug
- Donation of blood to a blood bank or in a clinical study (except a screening visit) within 4 weeks of study drug administration (within 2 weeks for plasma only)
Where it is running
- Wcct Global, Llc — Cypress, California, United States
Full record on ClinicalTrials.gov
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