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Clinical Trials/NCT00051038
NCT00051038
Completed
Phase 2

A Phase II Study of the Safety and Efficacy of Adding Entecavir to Current Lamivudine Therapy in HIV and HBV Co-Infected Patients Who Have Hepatitis B Viremia While Being Treated With Lamivudine

Bristol-Myers Squibb1 site in 1 countrySeptember 2002
ConditionsHepatitis B

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Hepatitis B
Sponsor
Bristol-Myers Squibb
Locations
1
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

The purpose of this clinical research study is to assess the safety and effectiveness of entecavir, when being added to lamivudine, in the treatment of adults with chronic hepatitis B infection who are co-infected with HIV.

Registry
clinicaltrials.gov
Start Date
September 2002
End Date
October 2005
Last Updated
15 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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