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Completed Phase 2 Interventional

A Comparison of Adefovir and Tenofovir for the Treatment of Lamivudine-Resistant Hepatitis B Virus in People With HIV

ClinicalTrials.gov ID: NCT00033163

Public ClinicalTrials.gov record NCT00033163. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 5:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Study identification

NCT ID
NCT00033163
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Enrollment
90 participants

Conditions and interventions

Interventions

  • Adefovir dipivoxil Drug
  • Tenofovir disoproxil fumarate Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Apr 30, 2005
Last update posted
Oct 31, 2021

Ends 2005

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
UC Davis Medical Center Sacramento California 95814
Univ. of California Davis Med. Ctr., ACTU Sacramento California
Ucsf Aids Crs San Francisco California 94110
University of Colorado Hospital CRS Aurora Colorado 80262
Northwestern University CRS Chicago Illinois 60611
Cook County Hosp. CORE Ctr. Chicago Illinois 60612
Johns Hopkins Adult AIDS CRS Baltimore Maryland 21287
Beth Israel Med. Ctr., ACTU New York New York 10003
NY Univ. HIV/AIDS CRS New York New York 10016
Cornell CRS New York New York 10021
Weill Med. College of Cornell Univ., The Cornell CTU New York New York
Univ. of Cincinnati CRS Cincinnati Ohio 452670405
MetroHealth CRS Cleveland Ohio 441091998
Vanderbilt Therapeutics CRS Nashville Tennessee 37203
University of Washington AIDS CRS Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00033163, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 31, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00033163 live on ClinicalTrials.gov.

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