The purpose of this study is to evaluate the safety, tolerability, drug levels, and drug effects of BMS-986308 compared to placebo in healthy participants.
Age range
18 Years – 55 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Incidence of Adverse Events (AEs)
Timeframe: Up to 19 days
Incidence of serious adverse events (SAEs)
Timeframe: Up to 19 days
Incidence of death
Timeframe: Up to 19 days
Incidence of adverse events (AEs) leading to discontinuation
Timeframe: Up to 19 days
Incidence of clinically significant changes in clinical laboratory results: Hematology tests
Timeframe: Up to 19 days
Incidence of clinically significant changes in clinical laboratory results: Clinical Chemistry tests
Timeframe: Up to 19 days
Incidence of clinically significant changes in clinical laboratory results: Urinalysis tests
Timeframe: Up to 19 days
Incidence of clinically significant changes in vital signs: Respiratory rate
Timeframe: Up to 19 days
Incidence of clinically significant changes in vital signs: Supine blood pressure
Timeframe: Up to 19 days
Incidence of clinically significant changes in vital signs: Heart rate
Timeframe: Up to 19 days
Incidence of clinically significant changes in vital signs: Orthostatic hypotension measurements performed as per clinical research unit's standard operating procedure
Timeframe: Up to 19 days
Incidence of clinically significant changes in electrocardiogram (ECG) parameters: PR interval
Timeframe: Up to 19 days
Incidence of clinically significant changes in electrocardiogram (ECG) parameters: QRS
Timeframe: Up to 19 days
Incidence of clinically significant changes in electrocardiogram (ECG) parameters: QT interval
Timeframe: Up to 19 days
Incidence of clinically significant changes in electrocardiogram (ECG) parameters: QTcF
Timeframe: Up to 19 days
Incidence of clinically significant changes in cardiac telemetry
Timeframe: Up to 19 days
Incidence of clinically significant changes in physical examination findings
Timeframe: Up to 19 days