An open-label, multiple-dosing, two-arms, one-sequence study to evaluate the safety and pharmacokinetics after co-administration of UIC201601 and UIC201602 in healthy male volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
40
* UIC201602 4 Cap/day for 14 days * Wash out 21 days * UIC201601 4 Tab + UIC201602 4 Cap / day for 14 days
* UIC201601 4 Tab/day for 7 days * Wash out 14 days * UIC201601 4 Tab + UIC201602 4 Cap / day for 14 days
Plasma pharmacokinetics(AUCss,τ) of UIC201602
Area under the serum drug concentration-time curve within a dosing interval at steady state
Time frame: 0 hour to 24 hours after Day 14 and Day 49 administration
Plasma pharmacokinetics(Css,max) of UIC201602
Maximum concentration of drug in serum at steady state
Time frame: 0 hour to 24 hours after Day 14 and Day 49 administration
Plasma pharmacokinetics(AUCss,τ) of UIC201601
Area under the serum drug concentration-time curve within a dosing interval at steady state
Time frame: 0 hour to 24 hours after Day 7 and Day 35
Plasma pharmacokinetics(Css,max) of UIC201601
Maximum concentration of drug in serum at steady state
Time frame: 0 hour to 24 hours after Day 7 and Day 35
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