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SGLT2i to Prevent of Liver Complications in Patients With CHB and Diabetes Mellitus
Sponsor: Chinese University of Hong Kong
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
Conditions
Interventions
Dapagliflozin 10mg Tab
Dapagliflozin 10mg Tab QD for 60 months.
Placebo 10mg Tab
Placebo 10mg Tab QD for 60 months.
Locations (1)
Prince of Wales Hospital
Hong Kong, Hong Kong