This study aims to evaluate the pharmacokinetics, pharmacodynamics, safety, and tolerability of DWP16001 in subjects with hepatic impairment compared with subjects with normal hepatic function.
The study design is An open-label, multi-center, parallel, single oral dose study.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
24
0.3mg
Seoul National University Hospital
Seoul, South Korea
RECRUITINGCmax of DWP16001
Cmax of DWP16001
Time frame: 0 to 48 hours
AUClast of DWP16001
AUClast of DWP16001
Time frame: 0 to 48 hours
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