drugset / Trial / NCT03969017

Combination Treatment of NAs and Peg IFN α-2b for Hepatitis B Related, Compensatory Cirrhosis Patients

NCT03969017

Phase 2 Unknown 84 enrolled Sun Yat-sen University
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The study aims to demonstrate that whether treatment of nucleoside (acid)analogues (NAs) plus pegylated interferon (Peg IFN) α-2b for those NAs treated, low level of HBsAg, hepatitis B related compensatory cirrhosis patients will result in higher HBsAg clearance rate and reduce the risk of liver cancer. The investigators plan to enroll about 84 hepatitis B related compensatory cirrhosis patients, who have received NAs treatment more than 1 year with the level of HBsAg \<1000IU/ml. These participants will be devided into 2 groups. Group A will receive the treatment of NAs plus Peg IFNα-2b. Group B will be treated with NAs as before enrollment. The participants in both groups will be followed up for 96 weeks. The primary endpoint is to compare the clearance rate of HBsAg between two groups. The secondary endpoint includes: (1) comparing the incidence of liver cancer during the 96 weeks follow-up, (2) comparing adverse side effects between the 2 groups. (3) comparing the virological and biochemical responses between the 2 groups.

Timeline

Start
2019-06-17
Primary completion
2022-05-30
Completion
2024-05-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Peginterferon alfa-2b Protein / enzyme biologic 90 ug
Subject Peginterferon alfa-2b Protein / enzyme biologic 135 ug
Subject Peginterferon alfa-2b Protein / enzyme biologic 180 ug
Background Entecavir Small molecule
Background Telbivudine Small molecule

Indications