This study aims to evaluate the effect of food on the pharmacokinetics and safety of DWP16001 after oral administration.
The study design is A randomized, Open-label, Oral, Single-dose, Two-way crossover study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
32
DWP16001 0.3mg
Chungbuk National University Hospital
Taebuk, South Korea
RECRUITINGAUC0-t of DWP16001
AUC0-t of DWP16001
Time frame: 0 to 72 hours
Cmax of DWP16001
Cmax of DWP16001
Time frame: 0 to 72 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.