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T cell count predicts the clinical efficacy of PegIFNa-2b in the treatment of CHB: a prospective study.

T cell count predicts the clinical efficacy of PegIFNa-2b in the treatment of CHB: a prospective study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108199
Enrollment
Unknown
Registered
2025-08-26
Start date
2025-08-26
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Chronic viral hepatitis B

Interventions

PegIFNa-2b treatment group:NA

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Voluntary enrollment, able to understand and sign the informed consent form; 2.At the time of signing the informed consent form, the age should be between 18 and 65 years old (including the boundary value), and there is no gender restriction. 3.HBsAg was positive during screening, and the history of HBsAg positivity was at least 6 months or there was other evidence suggesting CHB; 4.Interferon and other immunomodulators have not been used within 6 months prior to treatment; 5.The subjects denied pregnancy (women of childbearing age) and agreed to take effective contraceptive measures during the study period.

Exclusion criteria

Exclusion criteria: 1.Autoimmune liver disease, alcoholic hepatitis, drug-induced hepatitis, other viral hepatitis, moderate and severe steatohepatitis, decompensated liver disease and hepatocellular carcinoma; 2.There are other important organ diseases such as severe heart disease, uncontrolled diabetes, hypertension, thyroid disease, retinopathy, psychosis, autoimmune disease and epilepsy; 3.Autoimmune diseases, including psoriasis and systemic lupus erythematosus; 4.Confirmed or suspected liver cancer and other malignant tumors; 5.Unrequited alcoholics or drug addicts; 6.lactating women and those who plan to be pregnant within 2 years; 7.After organ transplantation or those who are ready for organ transplantation; 8.Those who are receiving immunosuppressant treatment; 9.Serum alanine aminotransferase level >10×ULN, total bilirubin level >2×ULN (anti-inflammatory and liver-protecting drugs should be used for at least 2 weeks); 10.Neutrophil count < 1.5×10^9/L and/or platelet count < 50× 10^9/L; 11.People who are allergic to research drugs (including PegIFNa-2b and NAs) or any of its components; 12.There are any contraindications in the instructions for drugs used in research; 13.Current infection with chronic infectious diseases such as hepatitis A, hepatitis C, hepatitis D, hepatitis E and HIV; 14.Other circumstances that the researcher thinks are not suitable for the group.

Design outcomes

Primary

MeasureTime frame
HBV RNA;T cell count;HBV-DNA quantification;HBsAg quantification;

Countries

China

Contacts

Public ContactLi Hong

West China Hospital of Sichuan University

anhong99999@163.com+86 28 85422650

Outcome results

None listed

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