drugset / Trial / NCT00523237
RAL-eve Study: Raltegravir Substitution Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Raltegravir | Other / unclassified | 400 mg | — |