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Phase 1
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18-55Altersgruppe
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Active, Not Recruiting
Active, Not Recruiting
A Study to Evaluate the Safety, Tolerability, Drug Levels, Food, Formulation, and pH Effects on Relative Absorption of BMS-986465 and Its Active Derivative BMS-986464 in Healthy Participants
The purpose of this study is to evaluate safety, tolerability, drug and food effects on relative bioavailability of BMS-986465 and its active derivative BMS-986464 in healthy participants and healthy participants of Japanese ethnicity.
Inclusion Criteria: - Healthy male and female (i e, women not of childbearing potential) participants - Body Mass Index (BMI) of 18 to 32 kg^m2 and total body weight ≥ 50 kg - Parts A, B, and D: Participants without restriction on ethnicity - Part C: Participants of Japanese ethnicity (both biological parents are ethnically Japanese) Exclusion Criteria: - Clinically significant medical, psychiatric and/or sound social reason, as determined by the investigator - Any major surgery within 3 months of study intervention administration - Participation in another clinical trial concurrent with this study Note: Other protocol-defined inclusion/exclusion criteria apply
Experimental: Part A: Single Ascending Dose (SAD) [BMS-986465 or placebo]
Experimental: Part B: Multiple Ascending Dose (MAD) [BMS-986465 or placebo, Pegasys]
Experimental: Part C: MAD in Japanese ethnicity [BMS-986465 or placebo]
Experimental: Part D: Food/Formulation/pH Effects [BMS-986465, Famotidine]