<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Teofilo E</submitter><funding>Bristol-Myers Squibb (France)</funding><pagination>17-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4975100</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Boosted protease inhibitors (PIs), including ritonavir-boosted atazanavir (ATV/r), are a recommended option for the initial treatment of HIV-1 infection based upon clinical trial data; however, long-term real-life clinical data are limited.&lt;h4>Objective&lt;/h4>We evaluated the long-term use of ATV/r as a component of antiretroviral combination therapy in the real-life setting in the REMAIN study.&lt;h4>Methods&lt;/h4>This was an observational cohort study conducted at sites across Germany, Portugal, and Spain. Retrospective historical and prospective longitudinal follow-up data were extracted every six months from medical records of HIV-infected treatment-naïve patients aged ≥ 18 years initiating a first-line ATV/r-containing regimen.&lt;h4>Results&lt;/h4>Eligible patients (n = 517) we</pubmed_abstract><journal>HIV clinical trials</journal><pubmed_title>Long-Term Efficacy, Tolerability, and Renal Safety of Atazanavir/Ritonavir-based Antiretroviral Therapy in a Cohort of Treatment-Naive Patients with HIV-1 Infection: the REMAIN Study.</pubmed_title><pmcid>PMC4975100</pmcid><funding_grant_id>Not applicable</funding_grant_id><pubmed_authors>Muller M</pubmed_authors><pubmed_authors>Jimenez-Exposito MJ</pubmed_authors><pubmed_authors>de Vilanova A</pubmed_authors><pubmed_authors>Karcher H</pubmed_authors><pubmed_authors>Teofilo E</pubmed_authors><pubmed_authors>Germano I</pubmed_authors><pubmed_authors>Freiwald M</pubmed_authors><pubmed_authors>Antela A</pubmed_authors><pubmed_authors>Mocho L</pubmed_authors><pubmed_authors>Gonzalez EO</pubmed_authors><pubmed_authors>Jessen H</pubmed_authors><pubmed_authors>de Suso MT</pubmed_authors><pubmed_authors>Pernia AT</pubmed_authors><pubmed_authors>Lauenroth-Mai E</pubmed_authors><pubmed_authors>Moreno Guillen S</pubmed_authors><pubmed_authors>Barros C</pubmed_authors><pubmed_authors>de Almeida J</pubmed_authors><pubmed_authors>Revuelta JA</pubmed_authors><pubmed_authors>Liano JP</pubmed_authors><pubmed_authors>Valente C</pubmed_authors><pubmed_authors>REMAIN study group</pubmed_authors><pubmed_authors>Vieira R</pubmed_authors><pubmed_authors>Fernandez PE</pubmed_authors><pubmed_authors>Santos C</pubmed_authors><pubmed_authors>Cid JF</pubmed_authors><pubmed_authors>Tavares L</pubmed_authors><pubmed_authors>Golz J</pubmed_authors><pubmed_authors>Schlote F</pubmed_authors><pubmed_authors>Mauss S</pubmed_authors><pubmed_authors>Aleixo MJ</pubmed_authors><pubmed_authors>Almeida L</pubmed_authors><pubmed_authors>Stoehr A</pubmed_authors><pubmed_authors>Gonzalez JS</pubmed_authors><pubmed_authors>Rocha-Pereira N</pubmed_authors><pubmed_authors>Serrao R</pubmed_authors><pubmed_authors>Schnaitmann E</pubmed_authors><pubmed_authors>Mayr C</pubmed_authors><pubmed_authors>Baumgarten A</pubmed_authors><pubmed_authors>Sanmartin LF</pubmed_authors><pubmed_authors>Santos J</pubmed_authors><pubmed_authors>Freud HK</pubmed_authors><pubmed_authors>Kern WV</pubmed_authors><pubmed_authors>Mansinho K</pubmed_authors><pubmed_authors>Meurer A</pubmed_authors><pubmed_authors>Sierra JO</pubmed_authors><pubmed_authors>Garcia JE</pubmed_authors><pubmed_authors>Comerma ED</pubmed_authors><pubmed_authors>Jimenez MC</pubmed_authors><pubmed_authors>Ameida I</pubmed_authors><pubmed_authors>Sala BC</pubmed_authors><pubmed_authors>Ferrer VF</pubmed_authors><pubmed_authors>Stellbrink HJ</pubmed_authors><pubmed_authors>Turmstraße P</pubmed_authors><pubmed_authors>Schuster D</pubmed_authors><pubmed_authors>Urbano J</pubmed_authors><pubmed_authors>Pedrol PD</pubmed_authors><pubmed_authors>Knechten H</pubmed_authors><pubmed_authors>Vera J</pubmed_authors><pubmed_authors>Aldeguer JL</pubmed_authors><pubmed_authors>de Orta G</pubmed_authors><pubmed_authors>Perez DG</pubmed_authors><pubmed_authors>Kuhlmann B</pubmed_authors><pubmed_authors>Cordes C</pubmed_authors><pubmed_authors>Audebert F</pubmed_authors><pubmed_authors>Rausch M</pubmed_authors><pubmed_authors>Oliveira C</pubmed_authors><pubmed_authors>Roxo F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long-Term Efficacy, Tolerability, and Renal Safety of Atazanavir/Ritonavir-based Antiretroviral Therapy in a Cohort of Treatment-Naive Patients with HIV-1 Infection: the REMAIN Study.</name><description>&lt;h4>Background&lt;/h4>Boosted protease inhibitors (PIs), including ritonavir-boosted atazanavir (ATV/r), are a recommended option for the initial treatment of HIV-1 infection based upon clinical trial data; however, long-term real-life clinical data are limited.&lt;h4>Objective&lt;/h4>We evaluated the long-term use of ATV/r as a component of antiretroviral combination therapy in the real-life setting in the REMAIN study.&lt;h4>Methods&lt;/h4>This was an observational cohort study conducted at sites across Germany, Portugal, and Spain. Retrospective historical and prospective longitudinal follow-up data were extracted every six months from medical records of HIV-infected treatment-naïve patients aged ≥ 18 years initiating a first-line ATV/r-containing regimen.&lt;h4>Results&lt;/h4>Eligible patients (n = 517) we</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Feb</publication><modification>2025-04-25T19:00:48.156Z</modification><creation>2019-03-27T02:20:03Z</creation></dates><accession>S-EPMC4975100</accession><cross_references><pubmed>26899539</pubmed><doi>10.1080/15284336.2015.1112494</doi></cross_references></HashMap>