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Functional Cure of Hepatitis B in HIV/HBV Co-infected Patients

G

Guangzhou Medical University

Status

Enrolling

Conditions

AIDS
Hepatitis B

Treatments

Drug: Peginterferon alfa-2b Injection

Study type

Observational

Funder types

Other

Identifiers

NCT05988879
GZ8H-202316253

Details and patient eligibility

About

Evaluate the potential of ART combined with interferon therapy to achieve functional cure of hepatitis B in HIV/HBV co-infected patients

Full description

This is a prospective, non-randomized, clinical observational cohort study. The subjects are the advantageous population for functional cure of hepatitis B in HIV/HBV co-infected patients . Depending on whether interferon therapy is used in the real world , the patients are divided into two groups: the ART combined with interferon group and the ART alone group, with 30 cases in each group. Hepatitis B surface antigen seroclearance rate and seroconversion rate will be observed during the study period.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18-65 years old, gender unrestricted.
  2. Meeting the People's Republic of China Health Industry Standard (WS293-2008) - "AIDS and HIV Infection Diagnostic Criteria", confirmed as HIV-1 infected.
  3. HBsAg positive for more than 6 months.
  4. At least 1 year of ART treatment prior to screening, and currently undergoing ART treatment with HBsAg <1000IU/mL, HBeAg negative, HBV DNA <100IU/ml, CD4+T lymphocyte count >200 cells/μL and HIV-RNA<20 copies/ml.

Exclusion criteria

  1. Pregnant, nursing, planning pregnancy, or with severe mental disorders or uncontrolled epilepsy.
  2. Co-infected with Hepatitis A, C, D, or E viruses.
  3. With other chronic liver diseases like autoimmune hepatitis, drug-induced hepatitis, alcoholic hepatitis, genetic metabolic liver diseases, or moderate to severe fatty liver.
  4. With autoimmune diseases like rheumatoid arthritis, psoriasis, or lupus.
  5. Post organ transplant, planning organ transplant, diagnosed or suspected of liver cancer or other malignant tumors, or undergoing immunosuppressive treatment.
  6. With severe diseases of heart, lungs, kidneys, brain, retinal disorders, or uncontrolled hypertension or diabetes.
  7. Excessive alcohol (average daily alcohol intake >40g for men, >20g for women) or drug users.
  8. Participated in other interventional trials within the last three months, or other situations deemed inappropriate for inclusion by researchers.

Trial design

60 participants in 2 patient groups

ART combined with interferon group
Description:
The treatment protocol is ART combined with pegylated interferon α-2b injection. The pegylated interferon α-2b injection is administered subcutaneously at a dose of 180ug once a week. Follow-up times are at baseline, and during treatment at weeks 4, 8, 12, 24, 36, 48, 60, and 72.
Treatment:
Drug: Peginterferon alfa-2b Injection
ART group
Description:
Continuously using ART treatment, without the use of interferon. Follow-up times are at baseline, and during treatment at weeks 12, 24, 36, 48, 60, and 72.

Trial contacts and locations

1

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Central trial contact

Yaozu He, Master; Linghua Li, PhD

Data sourced from clinicaltrials.gov

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