The trial was designed in a single dose, open, non-randomized, multi-dose parallel control group. The study of patients were mild and moderate renal insufficiency, and matched healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
18
Fasting oral test drug 12mg
West China Hospital of Sichuan University
Chengdu, China, China
Pharmacokinetic characteristics
Peak blood concentration (Cmax)
Time frame: 8 day
Pharmacokinetic characteristics
Area under the curve from 0 to the last time point t (AUC0-last)
Time frame: 8 day
Pharmacokinetic characteristics
Area under the curve from 0 to infinity (AUC0-inf)
Time frame: 8 day
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