TDF-FTC QD + Raltegravir BID TDF-FTC QD + Lopinavir-ritonavir QD

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Raltegravir vs. Lopinavir-ritonavir, both with 2NRTIs for nPEP RALPEP Trial

TDF-FTC QD + Raltegravir BID TDF-FTC QD + Lopinavir-ritonavir QD Raltegravir vs. Lopinavir-ritonavir, both with 2NRTIs for nPEP RALPEP: Study Design Study Design: RALPEP Background: Open label, prospective, randomized trial evaluating two regimens for post-exposure prophylaxis following sexual exposure Inclusion Criteria (n = 243) - Age > 18 - Recruited from hospital ER in Barcelona following potential sexual exposure to HIV Treatment Arms - TDF-FTC QD + Raltegravir 400 mg BID - TDF-FTC QD + Lopinavir-ritonavir 400-100 mg QD TDF-FTC QD + Raltegravir BID (n = 121) TDF-FTC QD + Lopinavir-ritonavir QD (n = 122) Source: Leal L, et al. J Antimicrob Chemother. 2016;71:1987-93.

Raltegravir vs. Lopinavir-ritonavir, both with 2NRTIs for nPEP RALPEP: Results 28-Day PEP Outcome Measures Source: Leal L, et al. J Antimicrob Chemother. 2016;71:1987-93.

Raltegravir vs. Lopinavir-ritonavir, both with 2NRTIs for nPEP RALPEP: Conclusions Conclusions: “Although we found no differences between arms regarding PEP non-completion, poor adherence and adverse events were significantly higher in patients allocated to tenofovir disoproxil/emtricitabine plus ritonavir-boosted lopinavir. These data support the use of raltegravir as the preferred third drug in current PEP recommendations.” Source: Leal L, et al. J Antimicrob Chemother. 2016;71:1987-93.