drugset / Trial / NCT00523237

RAL-eve Study: Raltegravir Substitution Study

NCT00523237

Completed 14 enrolled Stanford University
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to: * Provide raltegravir to subjects with HIV and an undetectable viral load who are experiencing injection site reactions (ISR) to Enfuvirtide, * Monitor the safety and efficacy of raltegravir, and * Assess the change in quality of life in patients who have switched from Enfuvirtide to raltegravir

Timeline

Start
2007-10
Primary completion
2009-03
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Raltegravir Other / unclassified 400 mg