Study to Evaluate the Safety, Tolerability, and Efficacy of ASC41 Tablets in Adult Patients With NASH

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

183

Participants

Timeline

Start Date

September 30, 2022

Primary Completion Date

May 10, 2025

Study Completion Date

June 10, 2025

Conditions
Non-alcoholic Fatty Liver DiseaseNon-alcoholic Steatohepatitis
Interventions
DRUG

2mg of ASC41

ASC41 tablet administered orally once daily.

DRUG

4mg of ASC41 (2 tablets of 2 mg ASC41)

ASC41 tablets administered orally once daily.

DRUG

Placebo

Placebo tablets administered orally once daily.

Trial Locations (1)

310000

The affiliated Hospital of Hangzhou Normal University, Hangzhou

Sponsors
All Listed Sponsors
lead

Gannex Pharma Co., Ltd.

INDUSTRY