ClinicalTrials.gg
RecruitingNCT07816094Updated Sep 11, 2026

Comparison of Viral Suppression With 0.5 mg and 1.0 mg Daily Doses of Entecavir in Decompensated HBV Cirrhosis of Liver

A Phase 4 interventional study of Entecavir in Hepatitis B, sponsored by Bangladesh Medical University. Recruiting at 1 site in Bangladesh. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-11.

Sponsored by Bangladesh Medical University · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Jan 2026, registered Sep 2026).
  • Started Jan 2026; still recruiting 10 months later.
Phase
Phase 4
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
18 Years and older
Sex
Male
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Study summary

This is a prospective, randomized, open-label clinical trial designed to compare the antiviral efficacy and safety of entecavir 0.5 mg once daily versus entecavir 1.0 mg once daily in adult patients with hepatitis B virus (HBV)-related decompensated liver cirrhosis. A total of 48 participants will be randomized equally to the two treatment groups and followed for 24 weeks. The primary outcome is the reduction in serum HBV DNA at week 24. Secondary outcomes include changes in Child-Pugh and MELD scores, HBeAg seroconversion, development or worsening of hepatic decompensation, occurrence of hepatocellular carcinoma, and safety of treatment.

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Conditions studied

  • Hepatitis B

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03

In context

Hepatitis B

1,045 studies on the registry are indexed under Hepatitis B; 139 are open to participants now.

This study's planned enrollment of 48 is below the median of 147 across 756 interventional studies indexed under Hepatitis B.

Browse Hepatitis B studies →

Lead sponsor

Bangladesh Medical University is the lead sponsor of 43 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age: 18 years or older.
  2. -related decompensated cirrhosis of liver based on clinical, biochemical and radiological evidence.
  3. Detectable level of HBV DNA irrespective of HBeAg status.

Exclusion criteria

Exclusion Criteria:

  1. Clinical, biochemical, or radiological evidence of hepatocellular carcinoma.
  2. Coinfection with .
  3. Patient is ongoing antiviral treatment.
  4. Cirrhosis due to other causes.
  5. Acute-on-chronic liver failure, defined according to the criteria established by APASL.
  6. Pregnancy.
  7. Patients with known or allergy to Entecavir.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
48 participants (estimated)

Study arms

  • Active comparator
    Entecavir 0.5 mg

    Participants receive Entecavir 0.5 mg orally once daily for 24 weeks.

    Drug: Entecavir

  • Active comparator
    Entecavir 1.0 mg

    Participants receive Entecavir 1.0 mg orally once daily for 24 weeks.

    Drug: Entecavir

Interventions

  • Participants receive oral Entecavir once daily. The dose is either 0.5 mg or 1.0 mg, according to randomized treatment assignment, 24 weeks.

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What researchers measure

Primary outcomes

  1. Change in Serum HBV DNA levels

    Comparison of the reduction in serum HBV DNA (IU/mL) from baseline to 24 weeks between receiving Entecavir 0.5 mg/day and 1.0 mg/day.

    Time frame: Baseline to Week 24

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Study locations

1 of 1 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07816094
Lead sponsor
Bangladesh Medical University
Responsible party
Hanif Uddin (MD Resident, Department of Hepatology, Bangladesh Medical University., Bangladesh Medical University) — Principal investigator
First posted
Sep 11, 2026
Start date
Jan 1, 2026
Primary completion
Jan 19, 2027 (estimated)
Completion
Jan 19, 2027 (estimated)
Last update
Sep 11, 2026

Study contacts

Hanif Uddin, MBBS
Contact
mdhanifuddin173@gmail.com
+8801710099830

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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