This study is to evaluate the single-dose pharmacokinetics (PK) and safety of Yimitasvir phosphate capsule in participants with End-stage renal disease without hemodialysis using matched healthy participants as a control group.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
16
DAG181 100 mg (100 mg Capsule) administered orally
West China Hospital of Sichuan University
Chengdu, Sichuan, China
Plasma pharmacokinetics (PK) parameters of DAG181 as measured by AUC
AUC is defined as the concentration of drug area under the curve
Time frame: From Days 1-5
Plasma pharmacokinetics (PK) parameters of DAG181 as measured by Cmax
Cmax is defined as the maximum concentration of drug
Time frame: From Days 1-5
Incidence of adverse events
The incidence of adverse events will be summarized
Time frame: From Days 1-5
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