drugset / Trial / NCT00224458

Combination of Efavirenz and Truvada - COMET Study

NCT00224458

Phase 4 Completed 400 enrolled Gilead Sciences
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To characterize the risks (safety and tolerability), effectiveness (continued viral load suppression and CD4 changes), and benefits (safety, tolerability, adherence, general satisfaction with the treatment regimen and QoL), of switching from a Combivir (BID) / efavirenz (QD) regimen to an all QD regimen of Truvada/efavirenz.

Timeline

Start
2004-09
Primary completion
Completion
2006-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Tenofovir Small molecule
Background Efavirenz Other / unclassified