drugset / Trial / NCT00791700

An Open Label Pharmacokinetic, Safety And Efficacy Study Of Maraviroc In Combination With Background Therapy For The Treatment Of HIV-1 Infected, CCR5 -Tropic Children

NCT00791700

Phase 2 Unknown 103 enrolled ViiV Healthcare Pfizer · collab
Parallel-groupOpen-labelTreatment

Summary

The primary purpose of this study is to determine the pharmacokinetic properties (what the body does to maraviroc) and to determine a suitable dosing schedule of maraviroc in HIV-1 infected children and adolescents. This study will also determine whether maraviroc is safe to use in children and adolescents.

Timeline

Start
2009-04-22
Primary completion
2015-04-14
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Maraviroc Other / unclassified