Abstract
Etravirine (Intelence®), an oral next-generation non-nucleoside reverse transcriptase inhibitor (NNRTI), is approved for the treatment of HIV-1 infection in treatment-experienced patients. In the US, the approved use of etravirine in patients who have evidence of viral replication and harbor HIV-1 strains resistant to other antiretroviral agents has recently been expanded to include pediatric patients aged ≥6 to <18 years. At 24 and 48 weeks in an open-label trial, etravirine 5.2mg/kg twice daily (maximum dosage 200 mg twice daily) plus an optimized background therapy regimen achieved complete viral response (defined as HIV-1 RNA <50 copies/mL) in approximately half of treatment-experienced children and adolescents with HIV-1 infection and evidence of viral replication, and had an acceptable tolerability profile.
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Acknowledgments and Disclosures
This article was reviewed by R. ter Heine, Department of Pharmacy and Pharmacology, Slotervaart Hospital, Amsterdam, the Netherlands.
The preparation of this article was not supported by any external funding. During the peer review process, the manufacturer of the agent under review was offered an opportunity to comment on the article. Changes resulting from comments received were made by the authors on the basis of scientific and editorial merit.
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Lyseng-Williamson, K.A. Etravirine: A Guide to Its Use in Treatment-Experienced Pediatric Patients with HIV-1 Infection in the US. Pediatr Drugs 14, 345–350 (2012). https://doi.org/10.1007/BF03262240
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DOI: https://doi.org/10.1007/BF03262240