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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.
Age
16 - No limit years
Sex
ALL
Healthy Volunteers
No
Local Investigator
Birmingham, Alabama, United States
Local Investigator
Tucson, Arizona, United States
Local Investigator
La Jolla, California, United States
Local Investigator
Los Angeles, California, United States
Local Investigator
Orange, California, United States
Local Investigator
San Francisco, California, United States
Local Investigator
Farmington, Connecticut, United States
Local Investigator
Miami Beach, Florida, United States
Local Investigator
Atlanta, Georgia, United States
Local Investigator
Honolulu, Hawaii, United States
Start Date
November 1, 2001
Primary Completion Date
May 1, 2005
Completion Date
May 1, 2005
Last Updated
April 14, 2011
Entecavir
DRUG
Lead Sponsor
Bristol-Myers Squibb
NCT06671093
NCT06885710
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06263959