Abstract
The fixed-dose combination of emtricitabine/tenofovir disoproxil fumarate (tenofovir DF) [Truvada®] is approved in the EU for pre-exposure prophylaxis, in conjunction with safer sex practices, to reduce the risk of sexually-acquired HIV-1 infection in adults at high risk. Once-daily administration of emtricitabine/tenofovir DF was effective in preventing HIV-1 infection in clinical trials in high-risk populations, including men who have sex with men, heterosexual HIV-1-serodiscordant couples, and heterosexual men and women. As adherence to the regimen correlates with the risk of HIV-1 infection, it is important that patient adhere to pre-exposure prophylaxis. Pre-exposure prophylaxis with the combination was generally well tolerated.
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Acknowledgements
The manuscript was updated from Drugs 2013;73(3):279–91 [45], and was reviewed by: T. Farazmandfer, Medical Cellular and Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran; S. McCormack, Medical Research Council, Clinical Trials Unit at University College London, London, UK; L. Van Damme, Global Health Program—HIV, Bill & Melinda Gates Foundation, Seattle (WA), USA. During the peer review process, the manufacturer of Truvada® was also offered an opportunity to review this article. Changes resulting from comments received were made on the basis of scientific and editorial merit.
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The preparation of this review was not supported by any external funding.
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E. Deeks, K.A. Lyseng-Williamson and G.L. Plosker are salaried employees of Adis/Springer, are responsible for the article content and declare no conflicts of interest.
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Deeks, E.D., Lyseng-Williamson, K. & Plosker, G.L. Emtricitabine/tenofovir disoproxil fumarate in HIV-1 pre-exposure prophylaxis: a guide to its once-daily use in the EU. Drugs Ther Perspect 33, 8–15 (2017). https://doi.org/10.1007/s40267-016-0363-9
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DOI: https://doi.org/10.1007/s40267-016-0363-9