Study on Clinical Program Optimization of Inactive Hepatitis B Surface Antigen (HBsAg) Carriers (IHCs)
Chronic Hepatitis B
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
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
Experimental
Experimental
Group A (continuous treatment group)
Group B (pulse therapy group)
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.