drugset / Trial / NCT00662545

Entecavir Intensification for Persistent HBV Viremia in HIV-HBV Infection

NCT00662545

RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate HIV-HBV infected individuals who have evidence of HBV replication in the blood after taking 48 weeks of more of the HBV active medication tenofovir in combination with emtricitabine or lamivudine. Eligible participants will be randomized to receive 24 weeks of entecavir (ETV) 1 mg versus continued standard of care antiretroviral therapy. After 24 weeks, individuals on entecavir or who remain HBV viremic on standard of care will receive ETV o for an additional 24 weeks. The hypothesis is that intensification with entecavir will reduce HBV DNA at 24 weeks more than continued antiretroviral therapy without entecavir.

Timeline

Start
2008-04
Primary completion
2010-02
Completion
2010-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Entecavir Small molecule 1 mg Oral
Comparator Lamivudine Other / unclassified
Comparator Tenofovir Small molecule
Comparator emtricitabine Other / unclassified