To Optimize the Therapeutic Pathway of Peginterferon Treatment in Patients With CHB Based on IFNA2p.Ala120Thr /ISGs. (IFNA2/ISGs)
Primary Purpose
Hepatitis B
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Nucleotide Analog
Interferon Alfa-2A
Sponsored by
About this trial
This is an interventional treatment trial for Hepatitis B focused on measuring Chronic Hepatitis B, IFNA2p.Ala120Thr /ISGs
Eligibility Criteria
Inclusion Criteria:
- Age between 18 and 65 years old;
- HBsAg positive, HBsAg quantification≤1500 IU/mL;
- Serum HBV DNA quantification <100 IU/mL;
- HBeAg negative.
Exclusion Criteria:
- Treated with interferon in the past six months;
- Liver cirrhosis or HCC and other associated tumors;
- Women during pregnancy or lactation;
- With liver disease caused by other causes;
- Combination infection of HIV or other immunodeficiency diseases;
- With diabetes, autoimmune diseases and other organ dysfunction or failure;
- Combination of other serious complications (infection, hepatic encephalopathy,gastrointestinal bleeding, hepatorenal syndrome, etc.);
- Others who cannot be treated with interferon;
- Anyone cannot return to the hospital for follow-up and follow-up visits regularly as planned
Sites / Locations
- Chan XieRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Active Comparator:NAs group
Experimental:PEG-IFN group
Arm Description
Active Comparator:nucleotide analogues(NAs) patients continue to use NAs
Experimental: peg-interferon alfa-2a patients use peg-interferon α-2a and nucleotide analogues(NAs)
Outcomes
Primary Outcome Measures
HBsAg clearance rate
Whether the HBsAg clearance rate of patients who received interferon treatment was higher than those treated with nucleoside drugs.
Secondary Outcome Measures
HBV cccDNA and pgRNA quantification dynamic change
The difference in cccDNA and pgRNA clearance rate between the two groups after 48 weeks of treatment in immune-controlled patients.
Full Information
NCT ID
NCT03771677
First Posted
December 8, 2018
Last Updated
May 4, 2023
Sponsor
Sun Yat-sen University
Collaborators
First People's Hospital of Foshan, Eighth Affiliated Hospital, Sun Yat-sen University
1. Study Identification
Unique Protocol Identification Number
NCT03771677
Brief Title
To Optimize the Therapeutic Pathway of Peginterferon Treatment in Patients With CHB Based on IFNA2p.Ala120Thr /ISGs.
Acronym
IFNA2/ISGs
Official Title
A Clinical Controlled Study to Optimize the Therapeutic Pathway of Peginterferon Alfa-2b Treatment in Patients With Chronic Hepatitis B Based on IFNA2p.Ala120Thr /ISGs Gene Spectrum.
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 1, 2018 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University
Collaborators
First People's Hospital of Foshan, Eighth 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
Yes
5. Study Description
Brief Summary
The study is to guide clinical cure of peginterferon alfa-2a treatment in patients with chronic hepatitis B based on the detection of interferon gene mutation (IFNA2p.Ala120Thr) and interferon-stimulated genes (ISGs) detection gene spectrum.
Detailed Description
It is estimated that more than 400 million people are infected with hepatitis B virus (HBV) globally.How to make more patients with chronic hepatitis B get clinical treatment through the existing anti-viral treatment is an urgent problem to be solved.This study is a random, multi-center and open experiment,the collaborators includes the second people's hospital of zhongshan city, the eighth people's hospital of guangzhou city, and the first people's hospital of foshan city.
Patients with chronic hepatitis B who were treated with NAs for over 1 year,HBsAg quantification≤1500 IU/mL, HBeAg negative and serum HBV DNA quantification <100 IU/mL were enrolled in this study. In our study, the enrolled patient's IFNA2p.Ala120Thr without variation and ISGs>0.05 were divided into two groups. After informed consent , patients were grouped according to their treatment intentions,in one group, patients continued NAs for another 48 weeks. In another group , patients were treated with peg-interferon-2a and NAs for 48 weeks.Patient's BMI, genotype, family history, smoking history, drinking history, other medical history, suspected transmission channels, types and time of use were recorded in this study.Moreover, Patients were assessed every 12 weeks,included liver and kidney function, blood routine, HBV cccDNA, HBeAg quantification, HBsAg quantification, pgRNA and so on.In addition,liver imaging examination and liver hardness test were assessed every six months.
In this study, we will analyze whether clinical cure rates differed between patients with chronic hepatitis B treated with peginterferon alfa-2a and NAs;Bisedes,the baseline interferon variant site variants and changes in interferon-stimulated gene profile expression were analyzed to determine whether they could be used as molecular markers to predict clinical cure with interferon.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B
Keywords
Chronic Hepatitis B, IFNA2p.Ala120Thr /ISGs
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Drug: nucleotide analogues(NAs)
Drug: Peginterferon alfa-2a and nucleotide analogues(NAs)
Masking
None (Open Label)
Masking Description
Active Comparator:nucleotide analogues(NAs) patients continue to use NAs
Experimental: peg-interferon alfa-2a patients switch to sequential peg-interferon α-2a
Allocation
Non-Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Active Comparator:NAs group
Arm Type
Active Comparator
Arm Description
Active Comparator:nucleotide analogues(NAs)
patients continue to use NAs
Arm Title
Experimental:PEG-IFN group
Arm Type
Experimental
Arm Description
Experimental: peg-interferon alfa-2a
patients use peg-interferon α-2a and nucleotide analogues(NAs)
Intervention Type
Drug
Intervention Name(s)
Nucleotide Analog
Other Intervention Name(s)
Nucleotide Analogs
Intervention Description
such as Entecavir,entecavir 0.5mg per day
Intervention Type
Drug
Intervention Name(s)
Interferon Alfa-2A
Other Intervention Name(s)
Pegasys
Intervention Description
Peginterferon alfa-2a 180ug per week
Primary Outcome Measure Information:
Title
HBsAg clearance rate
Description
Whether the HBsAg clearance rate of patients who received interferon treatment was higher than those treated with nucleoside drugs.
Time Frame
48 weeks
Secondary Outcome Measure Information:
Title
HBV cccDNA and pgRNA quantification dynamic change
Description
The difference in cccDNA and pgRNA clearance rate between the two groups after 48 weeks of treatment in immune-controlled patients.
Time Frame
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:
Age between 18 and 60 years old;
HBsAg positive, HBsAg quantification≤1500 IU/mL;
Serum HBV DNA quantification <100 IU/mL;
HBeAg negative.
Exclusion Criteria:
Treated with interferon in the past six months;
Liver cirrhosis or HCC and other associated tumors;
Women during pregnancy or lactation;
With liver disease caused by other causes;
Combination infection of HIV or other immunodeficiency diseases;
With diabetes, autoimmune diseases and other organ dysfunction or failure;
Combination of other serious complications (infection, hepatic encephalopathy,gastrointestinal bleeding, hepatorenal syndrome, etc.);
Others who cannot be treated with interferon;
Anyone cannot return to the hospital for follow-up and follow-up visits regularly as planned
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chan Xie, Professor
Phone
862085252043
Email
happyxiechan@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chan Xie
Organizational Affiliation
The Third Affliated Hospital of Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chan Xie
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chan Xie, Professor
Phone
862085252043
Email
happyxiechan@hotmail.com
12. IPD Sharing Statement
Learn more about this trial
To Optimize the Therapeutic Pathway of Peginterferon Treatment in Patients With CHB Based on IFNA2p.Ala120Thr /ISGs.
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