This is Open-label, Randomized, 3-sequence study to compare of pharmacokinetics and safety/tolerability profiles betweens DA-5206, a SR formulation of bepotastine besilate and Talion®, a IR formulation of bepotastine besilate under fasting and fed states in healthy male subjects
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Test drug l : DA-5206(Fasting)
Test drug ll : DA-5206(Fed)
Reference drug : Talion®
Korea University Anam Hospital
Seoul, South Korea
Area under the plasma concentration versus time curve (AUC)
PK Parameter
Time frame: 0~24hr
Peak Plasma Concentration (Cmax)
PK Parameter
Time frame: 0~24hr
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