CLINICAL TRIALS PROFILE FOR BMS-986166
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Clinical Trials for BMS-986166
Trial ID | Title | Status | Sponsor | Phase | Summary |
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NCT02790125 ↗ | A Randomized, Double Blind Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986166 in Healthy Subjects | Completed | Bristol-Myers Squibb | Phase 1 | The primary purpose of this study is to determine if single doses of BMS-986166 are safe and well tolerated in healthy male subjects and female subjects of non-childbearing potential. |
NCT03038711 ↗ | A Multiple Dose Study to Assess the Safety and Tolerability of BMS-986166 in Healthy Volunteers | Completed | Bristol-Myers Squibb | Phase 1 | The purpose of this study is to understand if multiple oral doses of BMS-986166 are safe and well tolerated in healthy patients. |
NCT04934696 ↗ | A Study to Characterize the Pharmacokinetics of an Oral Contraceptive With and Without BMS-986166 in Healthy Female Participants of Childbearing Potential | Recruiting | Bristol-Myers Squibb | Phase 1 | The purpose of this study is to investigate the potential for a drug-drug interaction (DDI) when BMS-986166 and hormonal oral contraceptives are co-administered. |
NCT04956627 ↗ | A Study to Assess the Effect of Itraconazole, Phenytoin, and Gemfibrozil on the Drug Levels of BMS-986166 in Healthy Participants | Recruiting | Bristol-Myers Squibb | Phase 1 | The purpose of this study is to evaluate the effect of itraconazole, phenytoin and gemfibrozil on the drug levels of BMS-986166 and its active metabolite BMT- 121795. Participants will be randomly assigned to one of four groups and will remain in the study clinic for the duration of treatment. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for BMS-986166
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Clinical Trial Locations for BMS-986166
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Clinical Trial Progress for BMS-986166
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Clinical Trial Sponsors for BMS-986166
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