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Effect of peginterferon a-2b on the conversion of HBeAg-negative chronic HBV infection patients with high HBsAg to the dominant population: an open-label study

Pegylated interferon a-2b induces the conversion of high-HBsAg HBeAg-negative chronic HBV infected patients to advantage population of functional cure: an open trial study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046859
Enrollment
Unknown
Registered
2021-05-29
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic hepatitis B

Interventions

Intervention group:peginterferon a-2b

Sponsors

The First People's Hospital of Yunnan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-60 years; 2. Positive HBsAg more than half a year with negative HBeAg and normal ALT, qHBsAg>3000IU/ml; 3. No antiviral treatment within six months before being selected; 4. For patients of childbearing age, agree to choose appropriate contraceptive measures (including at least one barrier contraceptive method) throughout the trial period; 5. Volunteer to join this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who have used hepatoprotective drugs within 1 month before being selected; 2. Serum anti-HIV positive; 3. Liver diseases caused by other causes 4. Patients who have progressed to liver cirrhosis or hepatocellular carcinoma; 5. Accompanied by serious or uncontrollable underlying diseases: such as infections, cardiovascular and cerebrovascular accidents, diabetes, epilepsy, rheumatoid arthritis, malignant tumors, etc.; 6. Pregnant and lactating women; 7. History of alcohol or drug abuse; 8. Participating in other hepatitis drug trials within 3 months or currently; 9. Subjects who are not suitable to participate in the research according to the researcher's judgment.

Design outcomes

Primary

MeasureTime frame
The ratio of qHBsAg<1500IU/ml;

Secondary

MeasureTime frame
Clearance of HBsAg;

Countries

China

Contacts

Public ContactGeng Jiawei

The First People's Hospital of Yunnan Province

617545329@qq.com+86 13888757766

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026