drugset / Trial / NCT01691794

Safety Sudy of Atazanavir Boosted With Ritonavir in the Treatment of HIV Infection in Pediatric Patients

NCT01691794

Phase 4 Completed 108 enrolled Bristol-Myers Squibb
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to collect safety clinical data in HIV-infected pediatric patients aged 6 and older to younger than18 years and weighing 15 kg or more, who are receiving atazanavir capsule boosted with ritonavir and an optimized nucleoside reverse transcriptase inhibitor backbone therapy as part of their antiretroviral regimen.

Timeline

Start
2012-11-30
Primary completion
2014-10-31
Completion
2017-02-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atazanavir Other / unclassified 150 mg
Comparator Atazanavir Other / unclassified 200 mg
Comparator Atazanavir Other / unclassified 300 mg
Comparator Ritonavir Other / unclassified 100 mg

Indications

No indication recorded.