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Study on Clinical Program Optimization of Inactive Hepatitis B Surface Antigen (HBsAg) Carriers (IHCs)

Primary Purpose

Chronic Hepatitis B

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
continuous treatment
pulse therapy
Sponsored by
Henan Provincial People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Hepatitis B focused on measuring inactive hepatitis B virus carriers, Pegylated Interferon α2b, Continuous treatment, pulse treatment

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age 18 to 65 years, both male and female (including 18 and 65 years old);
  • HBV DNA≤2000 IU/ml and HBeAg negative;
  • HBsAg positive for more than 6 months, and HBsAg≤1000 IU/ml;
  • ALT≤ULN at screening (discontinue liver-protecting enzyme-lowering drugs for at least 2 weeks);
  • A negative urine or serum pregnancy test (for women of childbearing age) within 24 hours before the first dose;
  • B-ultrasound or fibroscan suggest no liver cirrhosis;
  • Willing to accept treatment and sign informed consent.

Exclusion Criteria:

  • Participants with other hepatotropic viruses or human immunodeficiency virus co-infection;
  • other chronic non-viral liver diseases or decompensated liver diseases;
  • tumours;
  • drug abuse;
  • severe psychiatric disease;
  • uncontrolled thyroid disease or diabetes;
  • pregnancy or lactation.

Sites / Locations

  • Henan Provincial People's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group A (continuous treatment group)

Group B (pulse therapy group)

Arm Description

The treatment period is 12 weeks as a treatment unit, starting from the first day of baseline, subcutaneous injection of Peg-IFNα-2b 180μg once a week, the total treatment course does not exceed 96 weeks. During treatment, when any efficacy check point reaches the disappearance of HBsAg with or without the appearance of HBsAb, at least 2 treatment units of consolidation therapy are given and then the drug is discontinued. Observed for 24 weeks after treatment.

The treatment period is 12 weeks as a treatment unit. From the first day of baseline, subcutaneous injection of Peg-IFNα-2b 180 μg, every injection for 8 weeks, stop for 4 weeks, periodically, the total treatment course does not exceed 96 weeks. During treatment, when any efficacy check point reaches the disappearance of HBsAg with or without the appearance of HBsAb, at least 2 treatment units of consolidation therapy are given and then the drug is discontinued. Observed for 24 weeks after treatment.

Outcomes

Primary Outcome Measures

Extent of HBsAg decrease at 48 weeks
Decreasing level and difference of HBsAg in different treatment groups after 48 week treatment

Secondary Outcome Measures

HBsAg clearance at the end of 96 weeks of treatment
To determine the response rate will be evaluated by HBsAg loss defined as HBsAg level lower than 0.05 IU/ml after 96 week treatment
The decreasing extent of HBsAg level at 96 weeks
Decreasing level and difference of HBsAg in different treatment groups after 96 week treatment

Full Information

First Posted
July 11, 2022
Last Updated
July 13, 2022
Sponsor
Henan Provincial People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05457920
Brief Title
Study on Clinical Program Optimization of Inactive Hepatitis B Surface Antigen (HBsAg) Carriers (IHCs)
Official Title
The Efficacy and Safety of IHCs Treated With Pegylated Interferon α2b Based on Pulse Theray or Sequential Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2021 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
September 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Henan Provincial People's Hospital

4. Oversight

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

5. Study Description

Brief Summary
A multicenter, randomized controlled trial design was used to select patients with chronic hepatitis B in the immune control phase (i.e. HBsAg positive, HBeAg negative, normal ALT and HBsAg≤1000IU/ml, HBV DNA≤2000IU/ml) to enter this study, and to compare the feasibility, effectiveness and safety treated with Pegylated Interferon α2b Continuous therapy or Pulse therapy in immune-controlled chronic hepatitis B patients.
Detailed Description
Patients:chronic hepatitis B in the immune control phase (i.e. HBsAg positive, HBeAg negative, normal ALT and HBsAg≤1000IU/ml, HBV DNA≤2000IU/ml). The study patients were divided into two groups.Group A (PEG IFN α- 2b continuous group): PEG IFN was injected subcutaneously once a week from the first day of baseline α- 2b 180 μg. The total course of treatment should not exceed 96 weeks.Group B (PEG IFN α- 2b pulse group): from the first day of baseline, PEG IFN was injected subcutaneously α- 2b 180 μg. Every 8 weeks of injection, stop for 4 weeks, and conduct it periodically.Two groups at baseline, 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks, 48 weeks, 60 weeks, 72weeks, 84 weeks, 96 weeks and the 12th and 24th weeks after drug withdrawal, and corresponding examinations were carried out at each follow-up.Check and record adverse events and concomitant medication in detail, and evaluate the compliance of subjects; Blood samples were retained and transported to the laboratory for HBV at baseline, 24 weeks, 48weeks, 72, 96, and 12 and 24 after drug withdrawal.DNA quantification and detection of hepatitis B virus markers.The efficacy and safety were evaluated after the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis B
Keywords
inactive hepatitis B virus carriers, Pegylated Interferon α2b, Continuous treatment, pulse treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A (continuous treatment group)
Arm Type
Experimental
Arm Description
The treatment period is 12 weeks as a treatment unit, starting from the first day of baseline, subcutaneous injection of Peg-IFNα-2b 180μg once a week, the total treatment course does not exceed 96 weeks. During treatment, when any efficacy check point reaches the disappearance of HBsAg with or without the appearance of HBsAb, at least 2 treatment units of consolidation therapy are given and then the drug is discontinued. Observed for 24 weeks after treatment.
Arm Title
Group B (pulse therapy group)
Arm Type
Experimental
Arm Description
The treatment period is 12 weeks as a treatment unit. From the first day of baseline, subcutaneous injection of Peg-IFNα-2b 180 μg, every injection for 8 weeks, stop for 4 weeks, periodically, the total treatment course does not exceed 96 weeks. During treatment, when any efficacy check point reaches the disappearance of HBsAg with or without the appearance of HBsAb, at least 2 treatment units of consolidation therapy are given and then the drug is discontinued. Observed for 24 weeks after treatment.
Intervention Type
Behavioral
Intervention Name(s)
continuous treatment
Intervention Description
The treatment period is 12 weeks as a treatment unit, starting from the first day of baseline, subcutaneous injection of Peg-IFN α-2b 180μg once a week, or every 8 weeks of injection, 4 weeks off, periodically, the total treatment course does not exceed 96 weeks.
Intervention Type
Behavioral
Intervention Name(s)
pulse therapy
Intervention Description
pulse therapy
Primary Outcome Measure Information:
Title
Extent of HBsAg decrease at 48 weeks
Description
Decreasing level and difference of HBsAg in different treatment groups after 48 week treatment
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
HBsAg clearance at the end of 96 weeks of treatment
Description
To determine the response rate will be evaluated by HBsAg loss defined as HBsAg level lower than 0.05 IU/ml after 96 week treatment
Time Frame
96 weeks
Title
The decreasing extent of HBsAg level at 96 weeks
Description
Decreasing level and difference of HBsAg in different treatment groups after 96 week treatment
Time Frame
96 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age 18 to 65 years, both male and female (including 18 and 65 years old); HBV DNA≤2000 IU/ml and HBeAg negative; HBsAg positive for more than 6 months, and HBsAg≤1000 IU/ml; ALT≤ULN at screening (discontinue liver-protecting enzyme-lowering drugs for at least 2 weeks); A negative urine or serum pregnancy test (for women of childbearing age) within 24 hours before the first dose; B-ultrasound or fibroscan suggest no liver cirrhosis; Willing to accept treatment and sign informed consent. Exclusion Criteria: Participants with other hepatotropic viruses or human immunodeficiency virus co-infection; other chronic non-viral liver diseases or decompensated liver diseases; tumours; drug abuse; severe psychiatric disease; uncontrolled thyroid disease or diabetes; pregnancy or lactation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jia Shang
Phone
13938401888
Email
shangjia666@126.com
First Name & Middle Initial & Last Name or Official Title & Degree
Huibin Ning
Phone
15981849054
Email
situhailuo@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jia Shang
Organizational Affiliation
Henan Provincial People's Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Henan Provincial People's Hospital
City
Zhengzhou
State/Province
Henan
ZIP/Postal Code
450000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Huibin Ning
Phone
15981849054
Email
situhailuo@163.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
After publication
IPD Sharing Time Frame
End of study
IPD Sharing Access Criteria
Editors and reviewers of contributing magazines

Learn more about this trial

Study on Clinical Program Optimization of Inactive Hepatitis B Surface Antigen (HBsAg) Carriers (IHCs)

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