Actively Recruiting
Immunomodulatory Therapy and Predictors of Clinical Cure in Chronic Hepatitis B
Led by Peking University People's Hospital · Updated on 2026-01-09
132
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Achieving clinical cure, defined as hepatitis B surface antigen (HBsAg) seroclearance, represents a major research focus and an ideal therapeutic goal for chronic hepatitis B (CHB). A significant challenge in CHB management lies in promoting clinical cure, reducing relapse, and progressing towards complete cure. Studies have found that in patients who achieve HBsAg seroclearance following peginterferon alfa (PegIFNα) therapy, the seroconversion of anti-HBs and its attainment to a certain level are crucial for minimizing relapse. Strategies to promote anti-HBs seroconversion include active immunization (hepatitis B vaccine) and passive immunization (hepatitis B immunoglobulin, HBIG). Existing literature and preliminary findings from our team suggest that hepatitis B vaccine alone is ineffective in preventing relapse after clinical cure. This project proposes a multicenter, prospective, randomized controlled study. It will enroll CHB patients who have achieved HBsAg seroclearance with PegIFNα-based therapy, with the primary endpoint being the sustained HBsAg seroclearance rate at 48 weeks. The study will compare the efficacy between a group receiving HBIG immunization and a non-immunization control group. We anticipate that passive immunization with HBIG following HBsAg seroclearance will lead to a sustained clinical cure in CHB patients. This study aims to explore novel approaches for reducing relapse after clinical cure and pursuing complete cure, identify relevant biomarkers, and establish corresponding predictive models.
CONDITIONS
Official Title
Immunomodulatory Therapy and Predictors of Clinical Cure in Chronic Hepatitis B
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 to 60 years (inclusive).
- Documented HBsAg and/or HBV DNA positivity for over 6 months.
- Achieved HBsAg seroclearance (<0.05 IU/mL) following a PegIFNα-based treatment regimen.
- HBeAg negative and HBV DNA <10 IU/mL.
- Good compliance and willingness to voluntarily sign the informed consent form.
You will not qualify if you...
- Current decompensated cirrhosis or a history of decompensated cirrhosis.
- Individuals with spontaneous or Nucleos(t)ide analogue-induced HBsAg seroclearance.
- Coinfection with other viruses such as hepatitis A, C, D, E, or HIV.
- Severe other physical or mental illnesses including uncontrolled kidney, heart, lung, blood vessel, nervous system, digestive, or metabolic diseases; immunodeficiency; severe infections; active or past cancer.
- Use of corticosteroids, immunosuppressants, or chemotherapy within 6 months prior to enrollment or currently.
- Other liver diseases like alcoholic liver disease or autoimmune liver disease.
- Body Mass Index (BMI) greater than 28 kg/m².
- Any other condition that may reduce compliance or suitability for the study.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Peking University People's Hospital
Beijing, Beijing Municipality, China, 100044
Actively Recruiting
Research Team
B
Bo Feng
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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