The purpose of this clinical study is to evaluate the pharmacokinetics and safety of BR3409 and co-administration of BR3409-1 and BR3409-2 in healthy volunteers Under Fed Conditions
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Clinical Research Center, H PLUS Yangji Hospital
Seoul, Gwanakgu, South Korea
AUCτ
Area under the plasma drug concentration-time curve from 0 to time τ
Time frame: 0~48 hours after administration
Cmax
Maximum Concentration of Drug in Plasma
Time frame: 0~48 hours after administration
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