To evaluate and compare the safety and pharmacokinetic profiles of "AJU-G721" (test drug) and "G721R" (reference drug) in healthy adult male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
36
AJU-G721
G721R
Bumin Hospital
Seoul, South Korea
Cmax of Tamsulosin.
To assess the maximum observed plasma concentration (Cmax) of Tamsulosin.
Time frame: 0 hour ~ 48 hour after drug administration
AUCt of Tamsulosin
To assess the plasma concentration-time curve from time 0 to the last measurable concentration (AUCt) of Tamsulosin
Time frame: 0 hour ~ 48 hour after drug administration
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