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The Clinical Cure Project of Chronic Hepatitis B in China

Primary Purpose

Hepatitis B, Chronic

Status
Recruiting
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
pegylated interferon-alfa
Sponsored by
Third Affiliated Hospital, Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis B, Chronic

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

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

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

short-course combination group

full-course combination group

Monotherapy group

Arm Description

Nucleoside analogue is used during the first 3 months.

Nucleoside analogue is used during all the course of study.

Only Peg-IFN is used during all the course of study.

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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

Full Information

First Posted
July 13, 2019
Last Updated
April 11, 2023
Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
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1. Study Identification

Unique Protocol Identification Number
NCT04035837
Brief Title
The Clinical Cure Project of Chronic Hepatitis B in China
Official Title
A Study of Peg-interferon Treatment for Nucleos(t)Ide Analogues Suppressed Chronic Hepatitis B Patients With Low Level Hepatitis Surface Antigen
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 16, 2018 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Third Affiliated Hospital, Sun Yat-Sen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B, Chronic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
short-course combination group
Arm Type
Experimental
Arm Description
Nucleoside analogue is used during the first 3 months.
Arm Title
full-course combination group
Arm Type
Experimental
Arm Description
Nucleoside analogue is used during all the course of study.
Arm Title
Monotherapy group
Arm Type
Experimental
Arm Description
Only Peg-IFN is used during all the course of study.
Intervention Type
Drug
Intervention Name(s)
pegylated interferon-alfa
Intervention Description
All the patients in this study will receive pegylated interferon for all course.
Primary Outcome Measure Information:
Title
hepatitis B surface antigen
Description
hepatitis B surface antigen should be tested by the reagents from Roche or Abbott, which is expressed by using IU/ml.
Time Frame
up to 48 weeks
Secondary Outcome Measure Information:
Title
hepatitis B surface antibody
Description
hepatitis B surface antigen should be tested by the reagents from Roche or Abbott, which is expressed by using IU/ml.
Time Frame
up to 48 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhishuo Mo
Phone
+86 13632434363
Email
vbstone@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhiliang Gao
Organizational Affiliation
Third Affiliated Hospital, Sun Yat-Sen University
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Infectious Diseases, The Third Affliated Hospital of Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510630
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhi-Liang Gao, Professor
Phone
86-20-85252373
Email
zhilianggao@21cn.com
First Name & Middle Initial & Last Name & Degree
Xiang Zhu, Doctor
Phone
86-20-85252372
Email
0628zhuxiang@163.com
First Name & Middle Initial & Last Name & Degree
Zhi-Liang Gao, Professor

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Study protocol would be shared with other researchers.
Citations:
PubMed Identifier
18096267
Citation
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Citation
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PubMed Identifier
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Citation
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PubMed Identifier
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Citation
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Citation
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The Clinical Cure Project of Chronic Hepatitis B in China

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