Phase IIIB Study Evaluating the Effects of Atazanavir Powder With Ritonavir in HIV-infected Pediatric Patients
Completed · Phase 3
Conditions studied: HIV
In brief
The purpose of this study is to describe the safety, efficacy, and pharmacokinetics of a regimen of atazanavir powder boosted with ritonavir and an optimized dual nucleoside reverse transcriptase inhibitor in pediatric patients aged ≥3 months to \<11 years.
Key facts
- Study ID
- NCT01335698
- Run by
- Bristol-Myers Squibb
- People needed
- 160
- Starts
- 2011-05-27
- Expected to finish
- 2018-01-22
- Last updated by the study team
- 2018-11-09
Who can join
Age: 0 and older, up to 11. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Children'S National Medical Center — Washington D.C., District of Columbia, United States
- SUNY Upstate Medical University — Syracuse, New York, United States
- Local Institution — Buenos Aires, Bs As, Buenos Aires, Argentina
- Local Institution — Bunos Aires, Buenos Aires, Argentina
- Local Institution — Recife, Pernambuco, Brazil
- Local Institution — Porto Alegre, Rio Grande do Sul, Brazil
- Local Institution — Porto Alegre, Rio Grande do Sul, Brazil
- Local Institution — Ribeirão Preto, São Paulo, Brazil
- Local Institution — Santiago, Santiago Metropolitan, Chile
- Local Institution — Santiago, Santiago Metropolitan, Chile
- Local Institution — Guadalajara, Jalisco, Mexico
- Local Institution — Guadalajara, Jalisco, Mexico
- Local Institution — Df, Mexico City, Mexico
- Local Institution — Mérida, Yucatán, Mexico
- Local Institution — Oaxaca City, Mexico
- Local Institution — Puebla City, Mexico
- Local Institution — Warsaw, Poland
- Local Institution — Bucharest, Romania
- Local Institution — Saint Petersburg, Russia
- Local Institution — Saint Petersburg, Russia
- Local Institution — Smolensk, Russia
- Local Institution — Port Elizabeth, Eastern Cape, South Africa
- Local Institution — Port Elizabeth, Eastern Cape, South Africa
- Local Institution — Bloemfontein, Free State, South Africa
- Local Institution — Benoni, Gauteng, South Africa
Full record on ClinicalTrials.gov
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