CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed
Drug / intervention
Adefovir dipivoxil +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00033163
NCT00033163Phase 2Completed

A Randomized, Phase II, Controlled Trial Comparing the Efficacy of Adefovir Dipivoxil and Tenofovir Disoproxil Fumarate for the Treatment of Lamivudine-Resistant Hepatitis B Virus in Subjects Who Are Co-Infected With HIV

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Apr 9, 2002·Updated Nov 1, 2021

In Brief

A Phase 2 clinical trial evaluating Adefovir dipivoxil and Tenofovir disoproxil fumarate for HIV Infections and Hepatitis B. Completed, across 15 sites.

Detailed Summary

Control of hepatitis B virus (HBV) infection can be difficult in HIV infected people who have taken the antiviral lamivudine (3TC). These people may have HBV that has become resistant to 3TC. Adefovir dipivoxil (ADV) has shown promising anti-HBV activity in clinical trials; tenofovir disoproxil fumarate (TDF) is used to treat HIV and may also be effective against HBV. The purpose of this study is to find out if adding ADV or TDF to a highly active antiretroviral therapy (HAART) regimen that includes 3TC has an effect on HBV infection in patients coinfected with HIV and HBV. The tolerability and safety of these drugs will be examined.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedApr 9, 2002
Study CompletionMay 1, 2005
TodayJul 2, 2026
Posted 24.2 years ago

Interventions

Adefovir dipivoxildrug

Tenofovir disoproxil fumaratedrug