This study compares and evaluates the bioequivalence of AD-116A and AD-1161 in healthy adult male volunteers under fed conditions.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
44
H PLUS YANGJI HOSPITAL, Seoul
Seoul, South Korea
1. Area under the plasma concentration-time curve during dosing interval (AUCt)
AUCt of AD-116A
Time frame: [Time Frame: pre-dose (0hour) to 48hours]
2. Maximum concentration of drug in plasma (Cmax)
Cmax of AD-116A
Time frame: [Time Frame: pre-dose (0hour) to 48hours]
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