A Study to Evaluate the Safety and Pharmacokinetics of AD-231 Compared to Coadministration of AD-231A, AD-231D and AD-231C
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
AD-231 Oral Tablet
AD-231A Oral Tablet + AD-231D Oral Tablet + AD-231C Oral Tablet
H Plus Yangji Hospita
Seoul, South Korea
Maximum concentration of drug in plasma (Cmax)
Cmax
Time frame: pre-dose to 72 hours
Area under the plasma concentration-time curve during dosing interval (AUCt)
AUCt
Time frame: pre-dose to 72 hours
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