The purpose of this study is to investigate the effects of experimental medication BMS-986165 in healthy male participants.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
131
Specified dose on specified days
Specified dose on specified days
PRA Health Sciences
Salt Lake City, Utah, United States
Maximum plasma concentration (Cmax) of mycophenolic acid (MPA)
Time frame: 18 days
Area under the concentration vs time curve from time zero to the last quantifiable plasma concentration (AUC[0-T]) of MPA
Time frame: 18 days
AUC extrapolated to infinity (AUC[INF]) of MPA
Time frame: 18 days
Number of adverse events (AE)
Time frame: Up to 48 days
Number of serious adverse events (SAE)
Time frame: Up to 48 days
Number of AEs leading to discontinuation
Time frame: Up to 48 days
Incidence of clinically significant changes in laboratory test results, vital sign measurements, electrocardiograms (ECGs) and physical examination results
Time frame: 18 days
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