A Study to Assess Efficacy and Safety of HH-003 Injection in Subjects With Chronic Hepatitis Delta Virus Infection

PHASE2CompletedINTERVENTIONAL
Enrollment

101

Participants

Timeline

Start Date

June 16, 2023

Primary Completion Date

July 18, 2024

Study Completion Date

June 21, 2025

Conditions
Chronic Hepatitis Delta Virus Infection
Interventions
BIOLOGICAL

HH-003(20mg/kg)

20 mg/kg Q2W intravenously for 48 weeks

BIOLOGICAL

HH-003(10mg/kg)

10 mg/kg Q2W intravenously for 48 weeks

DRUG

TAF

TAF 25 mg QD orally during 48-week treatment period and 24-week follow-up period

Trial Locations (1)

100015

Beijing Ditan Hospital Captial Medical University, Beijing

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Huahui Health

INDUSTRY

NCT05861674 - A Study to Assess Efficacy and Safety of HH-003 Injection in Subjects With Chronic Hepatitis Delta Virus Infection | Biotech Hunter | Biotech Hunter