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NCT05182463RecruitingPhase 4

Peginterferon Treatment Study for Inactive Chronic Hepatitis B Patients

Real World Study of Peginterferon Alpha-2b Treatment for Inactive Chronic Hepatitis B Patients: E-Cure Study

Source: ClinicalTrials.gov · Last updated 1 May 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

There are about 400 million chronic hepatitis B virus (HBV) infection patients worldwide, posing a serious threat to global public health security. In China, HBV infection occured mainly in the perinatal period or infants, and about 10% of patients in the immune tolerance stage spontaneously transit to the immune clearance stage every year and become HBeAg-negative chronic HBV infection, resulting in a significant increase in the number of inactive chronic hepatitis B (CHB) patients. In recent years, different guidelines have not reached consensus on the need to initiate antiviral therapy for inactive CHB patients: In the guidelines of Asian Pacific Association for The Study of Liver(APASL)-2015 and American Association for the Study of Liver Diseases(AASLD)-2018, antiviral therapy is generally not recommended for this group of patients, and regular outpatient follow-up is recommended. Guideline of European Association for the Study of the Liver(EASL)-2017 suggests that people with a family history of cirrhosis and liver cancer at this stage could be treated with antiviral therapy even if they did not meet the indications of antiviral therapy. According to Guidelines for the Prevention and Treatment of Chronic Hepatitis B (version 2019) of China, antiviral therapy is still recommended for some patients with inactive HBsAg carrier status who are HBV DNA positive and meet the treatment indications. Studies have shown that some patients in immune tolerance stage may enter the immune clearance stage and have hepatitis flare. Patients of inactive CHB have the potential to develop HBeAg-negative CHB, and studies of long-term follow-up in this population have indicated the risk of hepatocellular carcinoma. With the popularization of the concept of functional cure for chronic hepatitis B, more and more people with inactive CHB have a strong desire for treatment. In recent years, several studies have demonstrated that Pegylated-interferon therapy can achieve high functional cure rate in patients with inactive CHB. The purpose of this study is to establish a national multi-center, prospective real world study to compare the efficacy of different antiviral treatment regimens for patients with inactive CHB and seek for the factors of functional cure.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
5000 (estimated)
First submitted
18 Dec 2021
Start date
8 Jan 2022
Primary completion date
13 Dec 2026
Lead sponsor
Third Affiliated Hospital, Sun Yat-Sen University
Diseases
Hepatitis B
NCT number
NCT05182463

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 5000
  • From 8 Jan 2022 to the primary completion date, 13 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients after or preparing for organ transplantation
  • Alcohol abuse (average alcohol intake is more than 40 g/d in males or 20g/d in women) or drug addicts

Other illness

  • Allergic to pegylated interferon α-2b
  • Coinfection with hepatitis A virus(HAV), hepatitis C virus(HCV), hepatitis D virus(HDV), hepatitis E virus(HEV) or human immunodeficiency virus(HIV)
  • Combined with other liver diseases (including drug-related, alcoholic, autoimmune, genetic metabolic liver diseases, etc.)
  • There are serious lesions in the important organs, such as heart, lung, kidney, brain and fundus
  • Patients with autoimmune diseases, unstable diabetes or thyroid diseases(hyperthyroidism or hypothyroidism)
  • Confirmed or suspected liver cancer or other malignant tumors
  • Present or past history of mental or psychological diseases
  • Other conditions that the investigators deem inappropriate for the study.

Lab values

  • Peripheral blood white blood cell count \< 3.5×109/L and/or platelet count \< 80×109/L

Other

  • Any indication of liver cirrhosis
  • Under immunosuppressant treatment
  • Pregnant or planned pregnancy in a short term or lactation patients

Who the study is looking for

  • Age 18-60, no gender limitation
  • HBsAg is positive for more than 6 months
  • Hepatitis B e antigen(HBeAg) is negative and anti-HBe is positive
  • Serum HBV DNA is less than 2000 IU/mL
  • Alanine aminotransferase(ALT) and/or Aspartate aminotransferase(AST) is normal
  • No antiviral durg (including nucleos(t)ide analogue and interferon) was used before enrollment
  • Good compliance and voluntarily signed informed consent

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Department of Infectious Diseases, The Third Affliated Hospital of Sun Yat-sen University
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.