Results of FEM-PrEP Clinical Trial Examining Pre-Exposure Prophylaxis (PrEP) for HIV Prevention Among Heterosexual WomenApril 18, 2011 Dear Colleague, Today, FHI announced that it will stop the FEM-PrEP study of pre-exposure prophylaxis (PrEP) for HIV prevention among heterosexual women. The decision was made after a regularly scheduled interim review of data by the trial's independent data monitoring committee determined that the trial could not demonstrate efficacy even if it continued to its originally-planned conclusion. These preliminary results are disappointing, especially given that this approach has already been shown to be effective in reducing HIV infection among men who have sex with men (MSM). The well-conducted study included nearly 2,000 women at high risk for HIV infection in three African nations and sought to determine if a once-daily pill containing oral tenofovir and emtricitabine (FTC/TDF or Truvada®) could protect women from HIV infection. Given today's results, CDC cautions against women using PrEP for HIV prevention at this time. We will not know if PrEP is effective for women, couples, or injection drug users until the conclusive results of this and other trials are reported. In the interim, CDC reiterates that daily PrEP with FTC/TDF has only been shown to be effective for HIV prevention among MSM. Interim CDC guidance on use among MSM is available here. For more information on today's FHI announcement, visit www.fhi.org. For CDC information on PrEP research and planning, visit www.cdc.gov/hiv/prep. Sincerely, Kevin A. Fenton, M.D., Ph.D. Jonathan H. Mermin, M.D., M.P.H. This article was provided by U.S. Centers for Disease Control and Prevention. Visit the CDC's website to find out more about their activities, publications and services.
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