drugset / Trial / NCT00116805

A Study to Compare Tenofovir Disoproxil Fumarate Versus Adefovir Dipivoxil for the Treatment of HBeAg-Positive Chronic Hepatitis B

NCT00116805 ↗

Phase 3 Completed 266 enrolled Gilead Sciences
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objectives of this study are to compare the efficacy, safety, and tolerability of tenofovir disoproxil fumarate (TDF) versus adefovir dipivoxil (ADV) for the treatment of HBeAg-positive chronic hepatitis B. Participants will receive TDF or ADV for 48 weeks (double-blind). After 48 weeks, eligible participants switched to open-label TDF for up to 480 weeks.

Timeline

Start
2005-06
Primary completion
2007-05
Completion
2016-01

Outcome

Met primary endpoint

paper significantly higher proportion of patients receiving tenofovir DF than of those receiving adefovir dipivoxil had reached the primary end point (P<0.001). PMID 19052126 ↗

registry NUMBER TDF-TDF: 66.5 percentage of participants NUMBER ADV 10 mg: 12.2 percentage of participants analysis (non-inferiority or equivalence test); TDF-TDF vs ADV 10 mg; p <0.001; Difference in proportions 54.1 (95% CI 44.6 to 63.6); Z-test NCT00116805 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adefovir dipivoxil Small molecule 10 mg Oral
Subject Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Background emtricitabine/tenofovir disoproxil fumarate Unknown 200 mg Oral
Background emtricitabine/tenofovir disoproxil fumarate Unknown 300 mg Oral