Assessment of Gut Absorption of Experimental Medication BMS-986165 in Healthy Males
Completed · Phase 1
Conditions studied: Psoriasis
In brief
The purpose of this study is to evaluate sites of gut absorption of BMS-986165 in males
Key facts
- Study ID
- NCT03873415
- Run by
- Bristol-Myers Squibb
- People needed
- 9
- Starts
- 2019-01-25
- Expected to finish
- 2019-05-01
- Last updated by the study team
- 2019-11-26
Who can join
Age: 18 and older, up to 45. Sex: male. Healthy volunteers: accepted.
You may qualify if…
- Body mass index of 18.0 to 32.0 kg/m2, inclusive, and weight ≥ 50 kg, at screening
- Estimated glomerular filtration rate (eGFR) > 80 mL/min/1.732 calculated with the Chronic Kidney Disease Epidemiology Collaboration formula
You may not qualify if…
- Any significant acute or chronic medical illness
- Current or recent (within 3 months of study drug administration) disease of the gut that, in the opinion of the Investigator or Medical Monitor, could impact upon the absorption of study drug
- Acute diarrhea, or constipation within 3 weeks prior to randomization
- Any major surgery within 4 weeks of randomization
- Other protocol defined inclusion/exclusion criteria could apply
Where it is running
- Scintipharma — Lexington, Kentucky, United States
Full record on ClinicalTrials.gov
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