<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Perez Stachowski J</submitter><funding>Gilead Sciences (Spain)</funding><funding>Gilead Sciences</funding><pagination>4994</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9457350</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(17)</volume><pubmed_abstract>Objective: The primary endpoint of the study was to determine the proportion of patients with HIV RNA &lt; 50 copies/mL at 48 weeks. Design: Phase IV, multicentric, open-label, single-arm clinical trial of participants recruited in 2018−2019 to evaluate the efficacy and safety of tenofovir alafenamide/emtricitabine/elvitegravir-cobicistat (TAF/FTC/EVG-c) as first-line treatment in HIV-1 infected naïve participants with advanced disease. Methods: Adverse events were graded according to the Division of AIDS scale version 2.0. Quantitative variables were recorded as median and interquartile range, and qualitative variables as absolute number and percentage. T-Student or Wilcoxon tests were used to analyze intragroup differences of the continuous variables. Results: Fifty participants were recrui</pubmed_abstract><journal>Journal of clinical medicine</journal><pubmed_title>Use of Tenofovir Alafenamide/Emtricitabine/Elvitegravir-Cobicistat in HIV-Naive Patients with Advanced Disease: GENIS Study.</pubmed_title><pmcid>PMC9457350</pmcid><funding_grant_id>IN-ES-292-4051</funding_grant_id><pubmed_authors>Ryan P</pubmed_authors><pubmed_authors>Nunez MJ</pubmed_authors><pubmed_authors>Dominguez M</pubmed_authors><pubmed_authors>Perez Stachowski J</pubmed_authors><pubmed_authors>Rial Crestelo D</pubmed_authors><pubmed_authors>Cabello N</pubmed_authors><pubmed_authors>Moreno Zamora A</pubmed_authors><pubmed_authors>Bisbal O</pubmed_authors><pubmed_authors>Vivancos Gallego MJ</pubmed_authors><pubmed_authors>Troya J</pubmed_authors><pubmed_authors>Espinosa Aguilera N</pubmed_authors><pubmed_authors>Sierra JO</pubmed_authors></additional><is_claimable>false</is_claimable><name>Use of Tenofovir Alafenamide/Emtricitabine/Elvitegravir-Cobicistat in HIV-Naive Patients with Advanced Disease: GENIS Study.</name><description>Objective: The primary endpoint of the study was to determine the proportion of patients with HIV RNA &lt; 50 copies/mL at 48 weeks. Design: Phase IV, multicentric, open-label, single-arm clinical trial of participants recruited in 2018−2019 to evaluate the efficacy and safety of tenofovir alafenamide/emtricitabine/elvitegravir-cobicistat (TAF/FTC/EVG-c) as first-line treatment in HIV-1 infected naïve participants with advanced disease. Methods: Adverse events were graded according to the Division of AIDS scale version 2.0. Quantitative variables were recorded as median and interquartile range, and qualitative variables as absolute number and percentage. T-Student or Wilcoxon tests were used to analyze intragroup differences of the continuous variables. Results: Fifty participants were recrui</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-21T14:15:11.665Z</modification><creation>2025-04-21T14:15:11.665Z</creation></dates><accession>S-EPMC9457350</accession><cross_references><pubmed>36078925</pubmed><doi>10.3390/jcm11174994</doi></cross_references></HashMap>