The primary objective of this study is to investigate the effect of multiple-dose administration of carbamazepine on the pharmacokinetics of S-892216 in healthy adults.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
16
S-892216 will be administered orally as a tablet.
Carbamazepine will be administered orally as a tablet.
ICON Lenexa
Lenexa, Kansas, United States
Plasma Concentration of S-892216
Time frame: Days 1 and 35 (2 hours predose, 30 minutes to 144 hours postdose)
Time to Maximum Plasma Concentration (Tmax) of S-892216
Time frame: Days 1 and 35 (2 hours predose, 30 minutes to 144 hours postdose)
Plasma Concentration of Carbamazepine
Time frame: Day 35 (2 hours predose, 30 minutes to 24 hours postdose)
Tmax of Carbamazepine
Time frame: Day 35 (2 hours predose, 30 minutes to 24 hours postdose)
Number of Participants Experiencing Treatment-emergent Adverse Events
Time frame: Day 1 through Day 49
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