The purpose of this study is to evaluate the safety, tolerability, and drug levels of BMS-986521 following single and multiple ascending doses of BMS-986521 in healthy adult participants, and to evaluate potential food effects on BMS-986521 exposure.
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Number of participants with treatment-emergent adverse events (AEs)
Timeframe: Up to approximately Day 40
Number of participants with treatment-emergent serious adverse events (SAEs)
Timeframe: Up to approximately Day 40
Number of participants with Treatment-emergent suicidal ideation and behavior as assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS)
Timeframe: Up to approximately Day 14
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