drugset / Trial / NCT01778413

Virological and Immunological Safety of a Dose Reduction Strategy Antiretroviral Regimen With Efavirenz / Tenofovir / Emtricitabine

NCT01778413

Phase 4 Completed 61 enrolled Anna Cruceta
RandomizedParallel-groupOpen-labelTreatment

Summary

The main objective is to determine the feasibility of maintaining virologic suppression on standard plasma viral load by dose reduction of ATRIPLA ®.

Timeline

Start
2013-06-03
Primary completion
2014-11-14
Completion
2015-07-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Atripla Unknown