drugset / Trial / NCT00089492

A Study Comparing the Efficacy and Safety of Once-Daily Fuzeon (Enfuvirtide) Dosing Versus the Currently Recommended Twice-Daily Dosing in Human Immunodeficiency Virus-Type 1 (HIV-1) Infected Patients

NCT00089492

Phase 2 Completed 64 enrolled Hoffmann-La Roche Trimeris · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will assess the safety and efficacy of once-daily administration of Fuzeon compared with twice-daily administration in HIV-1 infected patients who have received prior treatment. Patients will also receive an optimized treatment consisting of antiretroviral (ARV) therapy as determined by the treating physician. The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals.

Timeline

Start
2004-07
Primary completion
2006-06
Completion
2006-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Enfuvirtide Peptide 90 mg Subcutaneous
Comparator Enfuvirtide Peptide 180 mg Subcutaneous