drugset / Trial / NCT05382351

Antiviral Therapy for Patients With Chronic Hepatitis B Infection

NCT05382351

Phase 2 Unknown 238 enrolled Sun Yat-sen University
RandomizedParallel-groupSingle-blindTreatment

Summary

The study aims to demonstrate that antiviral therapy for patients with immune tolerance of CHB. On the basis of the original antiviral therapy of entecavir, further clarify the safety and effectiveness of entecavir combined with tenofovir amibufenamide.The investigators plan to enroll about 328 hepatitis B patients,. who are in the stage of immune tolerance. These participants will be devided into two groups randomly .Group A will receive the treatment of entecavir. Group B will be treated with entecavir and tenofovir amibufenamide. The participants in both groups will be followed up for 96 weeks. The primary endpoint is to compare the inhibition rate of HBV-DNA between two groups. The secondary endpoint includes: (1) Comparing the decrease of HBV DNA at 48 weeks between the two groups. (2) Comparing the HBeAg seroconversion rates at 48 weeks and 96 weeks between the two groups. (3) The changes of HBsAg at 48 weeks and 96 weeks between the two groups. (4) Comparing adverse side effects between the two groups.

Timeline

Start
2022-05-10
Primary completion
2024-04-30
Completion
2024-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tenofovir Amibufenamide Unknown 25 mg Oral
Background Entecavir Small molecule 0.5 mg Oral