Discontinuation of Antiviral Therapy as a Strategy to Cure Hepatitis B

NCT ID: NCT05328427

Last Updated: 2025-04-17

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 33 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-11-01
• Study Completion Date: 2026-06-30

Brief Summary

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.

Conditions

Hepatitis B, Chronic

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Stopping

Discontinuation of nucleoside analogue treatment

Group Type: ACTIVE_COMPARATOR

Stopping

Intervention Type: OTHER

Discontinuation of nucleoside analogue

Continue

Treatment with nucleoside analogue continued

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Stopping

Discontinuation of nucleoside analogue

Intervention Type: OTHER

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sahlgrenska University Hospital

OTHER

Sponsor Role: collaborator

Göteborg University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Infectious Diseases Clinic, Sahlgrenska University Hospital

Gothenburg, VGR, Sweden

Countries

Sweden

Other Identifiers

STOP-B

Identifier Type: -

Identifier Source: org_study_id