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Background: Antiretroviral therapy (ART) is recommended for all individuals with HIV infection, including those with acute HIV-1 infection (AHI). While recommendations are similar to those for chronic infection, efficacy data regarding treatment of acute HIV is limited.

Methods: This was a single arm, 96-week study of a once-daily integrase inhibitor (INSTI)-based regimen using elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (EVG/COBI/FTC/TDF) in AHI.

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Article Synopsis
  • Direct-acting antiviral agents (DAAs) have significantly improved the treatment of Hepatitis C (HCV), but an effective and safe treatment for patients co-infected with HIV remains a challenge, especially in low-resource settings.
  • This study evaluated the safety and efficacy of a 12-week treatment with sofosbuvir and velpatasvir in chronic HCV/HIV-1 co-infected patients who were already on an antiretroviral regimen.
  • Among 243 patients in the study, 97% achieved a sustained virologic response (SVR12) after treatment, demonstrating the high effectiveness of this regimen across different HCV genotypes.
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Article Synopsis
  • The study evaluated the effectiveness of switching HIV patients on stable antiretroviral therapy to a co-formulated drug called E/C/F/TDF, measuring success by the number of patients maintaining low viral loads at 48 weeks.
  • A total of 382 patients were analyzed, showing that 82% maintained viral loads below 50 copies/mL, while only 3.5% experienced virological failure, primarily linked to past treatment issues.
  • Resistance to integrase inhibitors was noted in those who failed treatment, though overall, the switch to E/C/F/TDF was well tolerated with minimal adverse effects reported.
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Objectives: Bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) is an effective treatment for HIV-1 infection; however, clinical trial data in older people living with HIV (PLWH) are lacking. The primary 24-week and secondary 48-week analyses of study GS-US-380-4449 (NCT03405935), which assessed the efficacy and safety of switching to B/F/TAF in older PLWH, have been published. Here we report the results of the final 96-week analyses from the study.

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Background: Efficacy of elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil (E/C/F/TDF) in treatment-naïve and experienced patients with HIV infection was demonstrated in phase 3 trials. The primary objective of this study was to evaluate effectiveness and safety of E/C/F/TDF in real world settings.

Methods: Retrospective, observational data collected by the Turkish ACTHIV-IST study group between May 2015 and December 2016 were analysed.

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