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A clinical study of peginterferon alfa-2b inducing immune tolerance patients to achieve immune activation

A clinical study of peginterferon alfa-2b inducing immune tolerance patients to achieve immune activation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046860
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:Pegylated Interferon Alpha-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. Age 18-60 years old; 2. Comply with the clinical diagnostic criteria in the "Guidelines for the Prevention and Treatment of Chronic Hepatitis B" (2019 Edition) regarding the immune tolerance period; 3. Have not received 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, such as hepatitis C, severe fatty liver, autoimmune liver disease, drug-induced hepatitis, etc.; 4. Patients who have progressed to liver cirrhosis or liver cancer; 5. Accompanied by serious or uncontrollable underlying diseases; 6. Pregnant and lactating women; 7. Suspected or do have a history of alcohol or drug abuse; 8. Those who are participating in other hepatitis drug trials within 3 months or currently; 9. Subjects who are unsuitable to participate in the research based on the researcher's judgment.

Design outcomes

Primary

MeasureTime frame
Seroconversion rates of HBeAg;

Secondary

MeasureTime frame
Complete virological response rate;

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