Pharmacokinetics and Safety Study of YZJ-1139 in Subjects With Mild, Moderate and Normal Hepatic Impairment

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

March 22, 2024

Primary Completion Date

April 18, 2024

Study Completion Date

August 7, 2024

Conditions
InsomniaHepatic Impairment
Interventions
DRUG

YZJ-1139

Single oral dose, 20 mg tablet

Trial Locations (1)

Unknown

The First Hospital of Jilin University, Changchun

All Listed Sponsors
lead

Shanghai Haiyan Pharmaceutical Technology Co., Ltd.

INDUSTRY

NCT06671509 - Pharmacokinetics and Safety Study of YZJ-1139 in Subjects With Mild, Moderate and Normal Hepatic Impairment | Biotech Hunter | Biotech Hunter