This is a study of experimental medication BMS-986036 given to healthy participants.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Crossover administration to abdomen then upper arm
PRA Health Sciences
Salt Lake City, Utah, United States
Maximum observed serum concentration (Cmax)
Time frame: 29 days
Time of maximum observed serum concentration (Tmax)
Time frame: 29 days
Area under the plasma concentration-time curve from time zero to time of last quantifiable concentration [AUC(0-t)]
Time frame: 29 days
Area under the plasma concentration-time curve from time zero extrapolated to infinite time [AUC(0-inf)]
Time frame: 29 days
Number of injection site reactions
Time frame: Up to 78 days
Number of adverse events (AE)
Time frame: Up to 78 days
Number of serious adverse events (SAE)
Time frame: Up to 78 days
Number of AEs leading to discontinuation
Time frame: Up to 78 days
Number of deaths
Time frame: Up to 78 days
Serum biomarker antibody concentration
Time frame: Up to 78 days
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