Abstract
Raltegravir is the first approved human immunodeficiency virus type 1 (HIV-1) integrase inhibitor; it targets the strand transfer step of HIV-1 integration. Clinical trials have demonstrated that raltegravir-containing regimens have potent anti- retroviral activity and are well tolerated in HIV-l-infected individuals. In antiretroviral treatment-experienced persons with drug-resistant HIV infection, raltegravir-containing treatment with an optimized background regimen was superior to an optimized background regimen alone. In treatment-naive persons, raltegravir was not inferior to efavirenz when the drugs were administered with tenofovir and lamivudine or emtricitabine. Raltegravir is metabolized by glucuronidation, not he- paticaHy; thus, the potential for drug-drug interactions is decreased. Drug resistance, conferred by substitutions in the gene coding for the HIV-1 integrase enzyme, develops relatively frequently after virologic failure. As an antiretroviral drug with a novel mechanism of action, raltegravir is an important advancement in HIV-1 treatment options. © 2009 by the Infectious Diseases Society of America. All rights reserved.
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CITATION STYLE
Hicks, C., & Gulick, R. M. (2009). Raltegravir: The first HIV Type 1 Integrase Inhibitor. Clinical Infectious Diseases, 48(7), 931–939. https://doi.org/10.1086/597290
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