To compare and evaluate the pharmacokinetic characteristics and the safety of fimasartan in hepatic impairment patients and healthy volunteers
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
18
single administration of fimasartan 120mg
single administration of fimasartan 120mg
Severance Hospital
Seoul, South Korea
Pharmacokinetic characteristics of fimasartan
AUC, Cmax, Tmax, T1/2, CL/F of fimasartan
Time frame: 0, 0.25, 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 16, 24, 32, 48h
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