To evaluate the drug-drug interaction of PK101-001 and PK101-002 in healthy volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
49
H Plus Yangji Clinical Research Center
Seoul, South Korea
AUCτ
Area under the plasma drug concentration-time curve for PK101-002 at Steady-state (between dose times)
Time frame: 0, 0.5, 1, 1.5, 2, 2.33, 2.67, 3, 3.5, 4, 6, 8, 12, 24, 36, 48 hour
Cmax,ss
The maximum (or peak) serum concentration for PK101-002 at Steady-state
Time frame: 0, 0.5, 1, 1.5, 2, 2.33, 2.67, 3, 3.5, 4, 6, 8, 12, 24, 36, 48 hour
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