The current study will estimate any inhibitive or inductive effect of PF-06651600 on the pharmacokinetics of midazolam and efavirenz.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
12
200 milligram (mg) PF-06651600 once daily (QD) orally for 11 days
single administration of midazolam 2 mg oral solution
single administration of efavirenz 50 mg capsule
Pfizer New Haven Clinical Research Unit
New Haven, Connecticut, United States
single dose Area under the curve at last quantifiable infinity time of midazolam
Time frame: Hour 0, 0,5, 1, 2, 4, 6, 8, 12, 16, 24 hours post-dose
Single dose Area under the Curve from time 0 to 72 hours post-dose of efavirenz
Time frame: hour 0, 0,5, 1, 2, 4, 6, 8, 12, 16, 24, 48, 72 hours post-dose
number of subjects with significant change from baseline in vital signs
Time frame: hour 0 on study days 1, 4, 10 and 13 post-dose
number of subjects with significant change from baseline in laboratory safety tests results
Time frame: study days -1, 4, 13 post-dose
number of subjects with treatment emergent adverse events (TEAE)
Time frame: Baseline up to 35 days post dose
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