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

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