Phase 4 Hepatitis B Trial, Recruiting NCT06364930 Sponsor: Chinese University of Hong Kong Condition: Hepatitis B
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Phase 4 Hepatitis B Trial, Recruiting

NCT06364930
Recruiting Phase 4

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have chronic hepatitis B and have been taking one of these antiviral medications (entecavir, tenofovir disoproxil fumarate, or tenofovir alafenamide) on its own for at least 12 months
  • You have been diagnosed with type 2 diabetes, or have blood sugar levels high enough to suggest diabetes or pre-diabetes (based on specific blood sugar or HbA1c test results — confirm with trial site)
  • You have been on the same diabetes medication(s) for the past three months without any changes
  • You have advanced liver scarring or signs of increased pressure in the liver's blood vessels, confirmed by specific scan or ultrasound measurements, or visible signs such as an enlarged spleen, fluid in the abdomen, or enlarged veins (confirm with trial site)
  • You are 18 years old or older
  • You are willing and able to give written consent to take part

Who may not be able to join:

  • You have hepatitis C, shown by a positive blood test for the hepatitis C virus
  • You have had serious complications from liver cirrhosis, or have been diagnosed with liver cancer
  • You have had an organ transplant
  • You are already taking a type of diabetes medication called an SGLT2 inhibitor (confirm with trial site for specific drug names)
  • Your kidneys are not working well enough (kidney filtration rate below a certain level — confirm with trial site)
  • Your blood sugar control is very poor, with an HbA1c level above 9.0%
  • You are taking three or more different diabetes medications
  • Your diabetes medications have been changed in the last three months
  • You have a serious illness or any form of cancer
  • You are under 18 years old
  • You are not willing or able to give consent to take part

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Principal Investigator: Grace LH Wong, MD, Chinese University of Hong Kong

Phone: +85235054205

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 4
Registry
ClinicalTrials.gov
Start date
26 March 2024
Est. completion
31 October 2030

Where this trial is recruiting

Hong Kong

Primary endpoints

The primary endpoint is liver complications

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov