Clinical Trial to evaluate the pharmacokinetic Characteristics, safety and Tolerability among CKD-215 and D215
A Multi-center, Randomized, Open-Label, Multiple-dose, Two-Stage, Two-treatment, Two-period, Crossover Study
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
AUCtau
Area under the plasma concentration-time curve over the dosing interval at steady state
Time frame: 0~12 hours
Css,max
Maximum observed plasma concentration at steady state
Time frame: 0~12 hours
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