The Clinical Cure Project of Chronic Hepatitis B in China

Sponsor
Third Affiliated Hospital, Sun Yat-Sen University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04035837
Collaborator
(none)
30,000
1
2
67.5
444.3

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Drug: pegylated interferon-alfa
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30000 participants
Allocation:
Non-Randomized
Intervention Model:
Sequential Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Study of Peg-interferon Treatment for Nucleos(t)Ide Analogues Suppressed Chronic Hepatitis B Patients With Low Level Hepatitis Surface Antigen
Actual Study Start Date :
May 16, 2018
Anticipated Primary Completion Date :
Dec 30, 2021
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: short-course combination group

Nucleoside analogue is used during the first 3 months.

Drug: pegylated interferon-alfa
All the patients in this study will receive pegylated interferon for all course.

Experimental: full-course combination group

Nucleoside analogue is used during all the course of study.

Drug: pegylated interferon-alfa
All the patients in this study will receive pegylated interferon for all course.

Outcome Measures

Primary Outcome Measures

  1. hepatitis B surface antigen [up to 48 weeks]

    hepatitis B surface antigen should be tested by the reagents from Roche or Abbott, which is expressed by using IU/ml.

Secondary Outcome Measures

  1. hepatitis B surface antibody [up to 48 weeks]

    hepatitis B surface antigen should be tested by the reagents from Roche or Abbott, which is expressed by using IU/ml.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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 Criteria:
  • Allergy to interferon

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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Infectious Diseases, The Third Affliated Hospital of Sun Yat-sen University Guangzhou Guangdong China 510630

Sponsors and Collaborators

  • Third Affiliated Hospital, Sun Yat-Sen University

Investigators

  • Study Chair: Zhiliang Gao, Third Affiliated Hospital, Sun Yat-Sen University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Zhiliang Gao, The director of the infectious diseases department, Third Affiliated Hospital, Sun Yat-Sen University
ClinicalTrials.gov Identifier:
NCT04035837
Other Study ID Numbers:
  • ZhuFeng Project
First Posted:
Jul 29, 2019
Last Update Posted:
Dec 22, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 22, 2021