This is a study of experimental medication BMS-986235 in healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
122
Specified dose on specified days
Specified dose on specified days
Anaheim Clinical Trials
Anaheim, California, United States
PRA Health Sciences
Salt Lake City, Utah, United States
Number of serious adverse events (SAE)
Time frame: Approximately 30 days
Number of deaths
Time frame: Approximately 30 days
Number of adverse events (AE) leading to study discontinuation
Time frame: Approximately 30 days
Number of patients with clinically significant changes in ECG parameters, as defined by the investigator
Time frame: Approximately 30 days
Number of patients with potentially clinically significant changes in vital signs
Time frame: Approximately 30 days
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