drugset / Trial / NCT00487188

A Study to Evaluate the Safety and Efficacy of Adding Enfuvirtide to Oral Highly Active Antiretroviral Therapy (HAART) in Human Immunodeficiency Virus (HIV) Patients With Prior Treatment Experience

NCT00487188

Phase 4 Completed 47 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

To assess the efficacy of enfuvirtide (Fuzeon) added to HAART compared to treatment with HAART alone in achieving and maintaining viral load suppression.

Timeline

Start
2005-11
Primary completion
2007-11
Completion
2008-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Enfuvirtide Peptide 90 mg Subcutaneous