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RECRUITING
NCT06364930
PHASE4

SGLT2i to Prevent of Liver Complications in Patients With CHB and Diabetes Mellitus

Sponsor: Chinese University of Hong Kong

View on ClinicalTrials.gov

Summary

This is a five-year, double blinded, randomised trial of dapagliflozin versus placebo in patients with chronic hepatitis B and DM or IFG complicated with compensated advanced chronic liver disease (cACLD). 412 subjects will be recruited. Subject will be randomly assigned to receive dapagliflozin 10mg daily or dapagliflozin placebo one tablet daily for up to 5 years. After randomization, subject will be followed up at month 3, month 6 and then 6-monthly until 60 months (follow up ± 4 weeks from scheduled clinic visit is allowed). At each visit, drug compliance, physical examination, observed or reported adverse events will be assessed. 10ml of blood will be taken at each visit and transient elastography to assess fibrosis regression will be performed at 60th month or at withdrawal visit. You are discouraged to use (pegylated)-interferon, any other NA including lamivudine, adefovir, and telbivudine, another SGLT2i Empagliflozin (Jardiance), Dapagliflozin + Metformin XR (Xigduo).

Official title: Sodium-glucose Co-transporter-2 Inhibitor (SGLT2i) to Prevent of Liver Complications in Patients With Chronic Hepatitis B and Diabetes Mellitus: a Double-blind, Randomised, Placebo-controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

412

Start Date

2024-03-26

Completion Date

2031-03-30

Last Updated

2026-03-18

Healthy Volunteers

No

Interventions

DRUG

Dapagliflozin 10mg Tab

Dapagliflozin 10mg Tab QD for 60 months.

DRUG

Placebo 10mg Tab

Placebo 10mg Tab QD for 60 months.

Locations (1)

Prince of Wales Hospital

Hong Kong, Hong Kong