The purpose of this study is to evaluate the effects of stomach acid suppression by rabeprazole and BMS-986165 on how fast and complete the drug is absorbed into the body of healthy participants.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
21
Specified dose on specified days.
Specified dose on specified days.
PRA Health Sciences - Netherlands
Groningen, Netherlands
Maximum Observed Plasma Concentration (Cmax) of BMS-986165
Time frame: Day 1 and Day 9
Area Under the Plasma Concentration-time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUC[0-T]) of BMS-986165
Time frame: Day 1 and Day 9
Area Under the Plasma Concentration-time Curve From Time Zero Extrapolated to Infinite Time (AUC[INF]) of BMS-986165
Time frame: Day 1 and Day 9
Percentage of Participants with Adverse Events (AEs)
Time frame: Up to Day 12
Percentage of Participants with Clinical Laboratory Values, Vital Signs, and Electrocardiograms (ECGs)
Time frame: Up to Day 12
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.