The Clinical Cure Project of Chronic Hepatitis B in China

Last updated: April 9, 2025
Sponsor: Third Affiliated Hospital, Sun Yat-Sen University
Overall Status: Active - Not Recruiting

Phase

4

Condition

Liver Disorders

Hepatitis B

Hepatitis

Treatment

pegylated interferon-alfa

Clinical Study ID

NCT04035837
ZhuFeng Project
  • Ages 18-60
  • All Genders

Study Summary

Chronic hepatitis B is a global public health problem, with nearly 700,000 deaths each year because of hepatitis B-related diseases. Recent studies have found that some patients who have used nucleot(s)ide analogues(NAs) for some period can achieve higher hepatitis B surface antigen(HBsAg) clearance rate(which is called clinical cure or functional cure) by using pegylated interferon. Patients who achieve clinical cure will further reduce liver inflammation, fibrosis and risks of liver cirrhosis and cancer in the future. This study was initiated in May 2018 and plans to recruit 30,000 eligible patients. The enrollment conditions are as follows: 1. according with the diagnosis of chronic hepatitis B in the guideline of China in 2015; 2.18-60 years old; 3. more than 1 year history of NAs therapy with HBsAg ≤1500 IU/ml, negative hepatitis e antigen and hepatitis B virus DNA<100 IU/ml; 4. no contraindications of interferon. For the above patients, pegylated interferon was used for 1-2 years(combined with NAs for at least 3 months).The primary goal of this study is to find out the optimal treatment for clinical cure.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • according with the diagnosis of chronic hepatitis B in the guideline of China in 2015

  • 18-60 years old

  • more than 1 year history of nucleot(s)ide analogues therapy with HBsAg ≤1500 IU/ml,negative HBeAg and HBV DNA<100 IU/ml

  • no contraindications of interferon

Exclusion

Exclusion Criteria:

  • Allergy to interferon

  • Alanine transaminase >10 times of upper limit of normal(ULN) or total bilirubin >2times of ULN

  • existing or previous decompensated liver cirrhosis

  • White blood cells or Platelet below the lower limit of normal

  • existing severe organ injury

  • combined with autoimmune diseases, psychiatric diseases, diabetes or thyroidism

  • confirmed or suspected malignant tumors

  • before or after transplantation

  • using immunosuppressor

  • pregnant or having a planned parenthood in 2 years

  • alcohol or drug addicted

  • infected by HIV

  • any conditions that is unsuitable to interferon therapy according to the doctors'judgement

Study Design

Total Participants: 30000
Treatment Group(s): 1
Primary Treatment: pegylated interferon-alfa
Phase: 4
Study Start date:
May 16, 2018
Estimated Completion Date:
June 30, 2026

Connect with a study center

  • Department of Infectious Diseases, The Third Affliated Hospital of Sun Yat-sen University

    Guangzhou, Guangdong 510630
    China

    Site Not Available

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