Safety and Pharmacokinetics/Pharmacodynamics of HSK3486 in Patients With Hepatic Impairment

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

November 14, 2019

Primary Completion Date

April 20, 2020

Study Completion Date

July 13, 2020

Conditions
Hepatic Impairment
Interventions
DRUG

HSK3486

HSK3486,Initially 0.4 mg/kg was administered as a 1 minute bolus, followed immediately by a constant infusion dose of 0.4 mg/kg/h administered as a 30 minute infusion via infusion pump.

Trial Locations (1)

130021

Phase I Clinical Trial Laboratory, The First Hospital of Jilin University, Changchun

All Listed Sponsors
collaborator

The First Hospital of Jilin University

OTHER

lead

Sichuan Haisco Pharmaceutical Group Co., Ltd

INDUSTRY

NCT04145596 - Safety and Pharmacokinetics/Pharmacodynamics of HSK3486 in Patients With Hepatic Impairment | Biotech Hunter | Biotech Hunter