The purpose of this study is to evaluate sites of gut absorption of BMS-986165 in males
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Oral administration
Scintipharma
Lexington, Kentucky, United States
Maximum observed plasma concentration (Cmax) of BMS-986165 following Treatments A, B, C, and D
Time frame: Determined over 5 days
Time of maximum observed plasma concentration (Tmax) of BMS-986165 following Treatments A, B, C, and D
Time frame: Determined over 5 days
Area under the plasma concentration-time curve from time zero to time of last quantifiable concentration [AUC(0-T)] of BMS-986165 following Treatments A, B, C, and D
Time frame: Determined over 5 days
Area under the plasma concentration-time curve from time zero extrapolated to infinite time [AUC(INF)] of BMS-986165 following Treatments A, B, C, and D
Time frame: Determined over 5 days
Apparent plasma elimination half-life (T-HALF) of BMS-986165 following Treatments A, B, C, and D
Time frame: Determined over 5 days
Vital signs of body temperature
Time frame: Up to 60 days
Pulse rate
Time frame: Up to 60 days
Physical examination
Time frame: Up to 60 days
Incidence of adverse events (AE)
Time frame: Up to 90 days
Incidence of serious adverse events (SAE)
Time frame: Up to 90 days
Vital sign of respiratory rate
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Time frame: Up to 60 days
Vital sign of supine blood pressure
Time frame: Up to 60 days