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Completed Phase 3 Interventional

A Phase III Study of Entecavir vs Lamivudine in Adults With Chronic Hepatitis B Infection and Negative for Hepatitis B e Antigen

ClinicalTrials.gov ID: NCT00035789

Public ClinicalTrials.gov record NCT00035789. 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 22, 2026, 6:36 PM EDT

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

Study identification

NCT ID
NCT00035789
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Entecavir Drug

Drug

Eligibility (public fields only)

Age range
16 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
Oct 31, 2001
Primary completion
Apr 30, 2005
Completion
Apr 30, 2005
Last update posted
Apr 13, 2011

2001 – 2005

United States locations

U.S. sites
31
U.S. states
23
U.S. cities
31
Facility City State ZIP Site status
Local Investigator Birmingham Alabama
Local Investigator Tucson Arizona
Local Investigator La Jolla California
Local Investigator Los Angeles California 90048
Local Investigator Orange California
Local Investigator San Francisco California
Local Investigator Farmington Connecticut
Local Investigator Miami Beach Florida
Local Investigator Atlanta Georgia 30322
Local Investigator Honolulu Hawaii
Local Investigator Chicago Illinois 60622
Local Investigator Iowa City Iowa
Local Investigator Kansas City Kansas
Local Investigator Dundalk Maryland
Local Investigator Worcester Massachusetts
Local Investigator Ann Arbor Michigan
Local Investigator Royal Oak Michigan
Local Investigator Saint Paul Minnesota
Local Investigator Manhasset New York
Local Investigator New York New York
Local Investigator Rochester New York
Local Investigator Charlotte North Carolina
Local Investigator Cleveland Ohio
Local Investigator Philadelphia Pennsylvania
Local Investigator Pittsburgh Pennsylvania
Local Investigator Providence Rhode Island
Local Investigator Nashville Tennessee 37211
Local Investigator Dallas Texas
Local Investigator Fairfax Virginia
Local Investigator Richmond Virginia
Local Investigator Seattle Washington

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 NCT00035789, 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 Apr 13, 2011 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00035789 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →