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Completed Phase 3 Interventional Results available

Telbivudine in Adults Previously Treated in Idenix-Sponsored Telbivudine Studies

ClinicalTrials.gov ID: NCT00142298

Public ClinicalTrials.gov record NCT00142298. 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 Sep 2, 2026, 10:27 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

An Open Label Trial of Telbivudine (LdT) in Adults With Chronic Hepatitis B Previously Treated in Idenix-Sponsored Telbivudine Studies

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is being conducted as an open-label, extended-term study for patients with chronic hepatitis B who have previously completed an Idenix-sponsored trial with telbivudine.

Study identification

NCT ID
NCT00142298
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,869 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
16 Years to 70 Years
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
Feb 28, 2005
Primary completion
Oct 31, 2009
Completion
Oct 31, 2009
Last update posted
Aug 20, 2020

2005 – 2009

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Novartis Investigational Site Phoenix Arizona 85001
Novartis Investigational Site Los Angeles California 90001
Novartis Investigational Site Los Angeles California 90073
Novartis Investigational Site Pasadena California 91103
Novartis Investigational Site Sacramento California
Novartis Investigational Site San Diego California 91945
Novartis Investigational Site San Francisco California 94115
Novartis Investigational Site Sarasota Florida
Novartis Investigational Site Atlanta Georgia
Novartis Investigational Site Honolulu Hawaii 96812
Novartis Investigational Site Chicago Illinois 60176
Novartis Investigational Site Boston Massachusetts 02215
Novartis Investigational Site Ann Arbor Michigan 48104
Novartis Investigational Site St Louis Missouri 63143
Novartis Investigational Site New York New York 10029
Novartis Investigational Site Chapel Hill North Carolina 27599-7211
Novartis Investigational Site Philadelphia Pennsylvania 19103
Novartis Investigational Site Houston Texas 77007
Novartis Investigational Site Richmond Virginia 23220

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00142298, 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 Aug 20, 2020 · Synced Sep 2, 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 NCT00142298 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →