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NCT Number: NCT05328427

Discontinuation of Antiviral Therapy as a Strategy to Cure Hepatitis B

Cirrhosis or cancer of the liver caused by hepatitis B virus (HBV) are major global health problems. Chronic HBV infection has become more common in Sweden with immigration. The risk of cancer and the availability of effective antivirals has led to more and more people receiving long-term treatment with antiviral drugs. The disadvantages of this treatment are that it does not have a defined duration and that it very rarely leads to the cure. Several published studies suggest that a large proportion of patients who discontinue antiviral therapy after at least three years may achieve lasting cure of the infection or at least do not need to resume treatment. The mechanism of this effect is not known, but it is thought to be due to the fact that the immune response, which is activated when the amount of virus increases after the end of treatment, becomes more effective in eradicating infected liver cells than it was before starting treatment. As a consequence of these findings updated guidelines for treatment of hepatitis B state that for patients that have received nucleoside analogue treatment for > 3 years, discontinuation is an accepted therapeutic alternative.

The purpose of the planned study is to investigate the results of discontinued treatment, in terms of clinical outcome as well as immunological and virological mechanisms. The aim is to include 120 patients at four regional infectious diseases clinics (in Gothenburg, Borås, Skövde and Trollhättan), of which 90 will be randomized to discontinue and 30 to continue antiviral treatment. Blood samples will be taken regularly to monitor the outcome and for detailed studies of viral antigens and nucleic acid in the blood and for specific analyzes of the cells of the immune system. The goal is to understand why the discontinued treatment in some patients activates an effective immune response and how such an effect can be predicted even before or early after the treatment is stopped.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Infectious Diseases Clinic, Sahlgrenska University Hospital

Gothenburg, VGR, 41650, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Nucleoside analogue treatment for HBeAg-negative chronic hepatitis B for at least 36 months.

Exclusion criteria

  • Liver cirrhosis or liver cancer.
  • Co-infection with HCV, HDV or HIV.
  • Inability to understand study information and give informed consent

Treatment and study plan

Stopping

Other

Discontinuation of nucleoside analogue

Primary outcomes

  1. HBsAg seronegativisation

    Time frame: 1 year

    Serum HBsAg becoming negative

  2. HBsAg seronegativisation

    Time frame: 2 years

    Serum HBsAg becoming negative

  3. HBsAg reduction

    Time frame: 1 year

    HBsAg reduction by > 1 log IU/mL

  4. HBsAg reduction

    Time frame: 2 years

    HBsAg reduction by > 1 log IU/mL

  5. Clinical responder

    Time frame: 2 years

    Sustained HBV DNA < 2000 IU/mL and normal ALT

Secondary outcomes

  1. HBV-specific T cell activation

    Time frame: After 16 weeks

    Activation of HBV-specific T-cell responses, induced by incubating whole blood with HBV-core and HBsAg derived peptides for 48 hours, and investigated by measuring gamma interferon, chemokine and cytokine levels in plasma after centrifugation of the stimulated whole blood.

Sponsors and collaborators

Lead sponsor

Göteborg University

Other

Collaborators

  • Sahlgrenska University Hospital

Registry information

Acronym: STOP-B

Important dates

Study start
2022
Primary completion
2024
Study completion
2026
First posted
Apr 14, 2022
Registry last updated
Apr 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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