drugset / Trial / NCT00162227

An Expanded Access Study of Oral Liquid Efavirenz in the Treatment of Children With HIV Infection

NCT00162227

Expanded access No longer available Bristol-Myers Squibb

Summary

This study is being conducted to assess the safety and tolerability of an oral liquid solution of Sustiva for antiretroviral therapy-naive or therapy-experienced HIV-1 infected children between the ages 3-16 who are failing or intolerant of current antiretroviral regimen and who are unable to swallow Sustiva capsules.

Timeline

Start
2000-09
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Efavirenz Other / unclassified 200 mg Oral
Subject Efavirenz Other / unclassified 600 mg Oral