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Chronic Hepatitis BPhase 3NCT00035789

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

A Phase 3 study testing Entecavir in people with Chronic Hepatitis B, run by Bristol-Myers Squibb at 31 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this clinical research study is to assess the safety and effectiveness of entecavir, as compared to lamivudine, in the treatment of adults with chronic hepatitis B infection who are hepatitis B e antigen negative. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Chronic Hepatitis B
What is being tested?
Entecavir
How many people
Not given
Where
31 sitesUnited States
Study dates
Nov 2001to May 2005
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult
  • Male and female subjects =/> 16 years of age (or minimum age required in a given country) with history of chronic hepatitis B infection;
  • HBeAg negative, anti-HBeAb positive;
  • Absence of coinfection with human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis D virus (HDV);
  • Absence of other forms of liver disease e.g., alcoholic, autoimmune, biliary disease;
  • Less than 12 weeks prior therapy with nucleoside or nucleotide analogue antiviral agents with activity against hepatitis B (e.g., adefovir, famciclovir and lamivudine)

Trial locations and contacts

31 sites in 1 country.

31 sites in 1 country

United States31 sites
  • Local Investigator

    Ann Arbor, Michigan

  • Local Investigator

    Atlanta, Georgia, 30322

  • Local Investigator

    Birmingham, Alabama

  • Local Investigator

    Charlotte, North Carolina

  • Local Investigator

    Chicago, Illinois, 60622

  • Local Investigator

    Cleveland, Ohio

  • Local Investigator

    Dallas, Texas

  • Local Investigator

    Dundalk, Maryland

  • Local Investigator

    Fairfax, Virginia

  • Local Investigator

    Farmington, Connecticut

  • Local Investigator

    Honolulu, Hawaii

  • Local Investigator

    Iowa City, Iowa

  • Local Investigator

    Kansas City, Kansas

  • Local Investigator

    La Jolla, California

  • Local Investigator

    Los Angeles, California, 90048

  • Local Investigator

    Manhasset, New York

  • Local Investigator

    Miami Beach, Florida

  • Local Investigator

    Nashville, Tennessee, 37211

  • Local Investigator

    New York, New York

  • Local Investigator

    Orange, California

  • Local Investigator

    Philadelphia, Pennsylvania

  • Local Investigator

    Pittsburgh, Pennsylvania

  • Local Investigator

    Providence, Rhode Island

  • Local Investigator

    Richmond, Virginia

  • Local Investigator

    Rochester, New York

  • Local Investigator

    Royal Oak, Michigan

  • Local Investigator

    Saint Paul, Minnesota

  • Local Investigator

    San Francisco, California

  • Local Investigator

    Seattle, Washington

  • Local Investigator

    Tucson, Arizona

  • Local Investigator

    Worcester, Massachusetts

Other trials in United States

About this study

The purpose of this clinical research study is to assess the safety and effectiveness of entecavir, as compared to lamivudine, in the treatment of adults with chronic hepatitis B infection who are hepatitis B e antigen negative.

Being tested
Entecavir
Medical subject headings
Hepatitis B, Chronic

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • EntecavirDrug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 May 2002 (estimated)
  2. Study startNov 2001
  3. Primary completionMay 2005
  4. Study completionMay 2005

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
IDs, dates and publications
ClinicalTrials.gov ID
NCT00035789
Sponsor's protocol ID
AI463-027
Status last verified
Jan 2010
First submitted
5 May 2002
Last updated
14 Apr 2011
Results posted
No

Publications

  • Lai CL, Shouval D, Lok AS, Chang TT, Cheinquer H, Goodman Z, DeHertogh D, Wilber R, Zink RC, Cross A, Colonno R, Fernandes L; BEHoLD AI463027 Study Group. Entecavir versus lamivudine for patients with HBeAg-negative chronic hepatitis B. N Engl J Med. 2006 Mar 9;354(10):1011-20. doi: 10.1056/NEJMoa051287.

    PubMed 16525138

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Entecavir in people with Chronic Hepatitis B, run by Bristol-Myers Squibb at 31 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Apr 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 31 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00035789, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Apr 2011; AzTrials last refreshed its copy on 8 Nov 2026.

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