Gilead Receives European Marketing Authorization for Eviplera
The authorization allows for the commercialization of Eviplera in all 27 countries of the European Union.
Gilead Sciences, Inc. announced yesterday that the European Commission has granted marketing authorization for Eviplera? (emtricitabine/rilpivirine/tenofovir disoproxil), a complete once-daily single-tablet regimen for the treatment of HIV-1 infection in antiretroviral treatment-na?ve adults with a viral load less than or equal to 100,000 HIV-1 RNA copies/mL.
The authorization allows for the commercialization of Eviplera in all 27 countries of the European Union (EU).
Dr. Mark Nelson, Service Director for the HIV Directorate, Chelsea and Westminster Hospital, London, United Kingdom, said,“Eviplera has the potential to be an important new treatment option for patients starting HIV therapy because it streamlines an effective HIV treatment regimen into a
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