<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(2)</volume><submitter>Leal L</submitter><pubmed_abstract>In 2020, COVID-19 caused a global health crisis, prompting research efforts and accelerating drug development. As part of this response, we conducted a phase 2b, multicentre, open-label, randomized (1:1) clinical trial to compare the effects of siltuximab versus corticosteroids on disease progression in hospitalized adults with COVID-19 pneumonia. Between April 2020 and January 2021, 82 patients were randomized to receive siltuximab and 80 corticosteroids (20 methylprednisolone and 60 dexamethasone). Median (IQR) age was 61 years (50-72). Nineteen patients allocated to siltuximab were admitted to the intensive care unit compared to eight receiving corticosteroids (p = 0.025). Corticosteroid treatment was independently associated with a higher risk of avoiding intensive care unit admission </pubmed_abstract><journal>Clinical and translational science</journal><pagination>e70491</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12874496</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effects of Siltuximab Versus Corticosteroids in Preventing COVID-19 Pneumonia Disease Progression: Multicentre, Open-Label, Randomized Clinical Trial.</pubmed_title><pmcid>PMC12874496</pmcid><pubmed_authors>Carbonell I</pubmed_authors><pubmed_authors>Vergara A</pubmed_authors><pubmed_authors>Paredes R</pubmed_authors><pubmed_authors>Castro P</pubmed_authors><pubmed_authors>Laguno M</pubmed_authors><pubmed_authors>Segui F</pubmed_authors><pubmed_authors>Marco-Hernandez J</pubmed_authors><pubmed_authors>Pich J</pubmed_authors><pubmed_authors>Chumbita M</pubmed_authors><pubmed_authors>Puerta-Alcalde P</pubmed_authors><pubmed_authors>Padrosa J</pubmed_authors><pubmed_authors>Castan C</pubmed_authors><pubmed_authors>Ferrer E</pubmed_authors><pubmed_authors>Gonzalez-Cordon A</pubmed_authors><pubmed_authors>Rico V</pubmed_authors><pubmed_authors>SILCOR study group</pubmed_authors><pubmed_authors>Fernandez S</pubmed_authors><pubmed_authors>Soriano A</pubmed_authors><pubmed_authors>Calvo J</pubmed_authors><pubmed_authors>Muelas M</pubmed_authors><pubmed_authors>Marcos MA</pubmed_authors><pubmed_authors>Rojas J</pubmed_authors><pubmed_authors>Camprubi D</pubmed_authors><pubmed_authors>Lopez-Soto A</pubmed_authors><pubmed_authors>Sola M</pubmed_authors><pubmed_authors>Dalmau D</pubmed_authors><pubmed_authors>Almuedo A</pubmed_authors><pubmed_authors>Garcia F</pubmed_authors><pubmed_authors>Ventosa H</pubmed_authors><pubmed_authors>Feliu M</pubmed_authors><pubmed_authors>Tuset M</pubmed_authors><pubmed_authors>de Alba MT</pubmed_authors><pubmed_authors>Bodro M</pubmed_authors><pubmed_authors>Capdevila A</pubmed_authors><pubmed_authors>Gabara C</pubmed_authors><pubmed_authors>Carbonell C</pubmed_authors><pubmed_authors>Garcia-Vidal C</pubmed_authors><pubmed_authors>Ribot J</pubmed_authors><pubmed_authors>Naval J</pubmed_authors><pubmed_authors>Tellez A</pubmed_authors><pubmed_authors>Rodriguez N</pubmed_authors><pubmed_authors>Matas A</pubmed_authors><pubmed_authors>Aldea A</pubmed_authors><pubmed_authors>Pinazo MJ</pubmed_authors><pubmed_authors>Ladino A</pubmed_authors><pubmed_authors>de Lazzari E</pubmed_authors><pubmed_authors>Del Puerto Bernoy Gonzalez M</pubmed_authors><pubmed_authors>Martinez JA</pubmed_authors><pubmed_authors>Aguero D</pubmed_authors><pubmed_authors>Moreno A</pubmed_authors><pubmed_authors>Meira F</pubmed_authors><pubmed_authors>Del Rio A</pubmed_authors><pubmed_authors>Garcia-Pouton N</pubmed_authors><pubmed_authors>Munoz J</pubmed_authors><pubmed_authors>Ambrosioni J</pubmed_authors><pubmed_authors>Rubio E</pubmed_authors><pubmed_authors>Hernandez-Meneses M</pubmed_authors><pubmed_authors>Pellice M</pubmed_authors><pubmed_authors>Marti H</pubmed_authors><pubmed_authors>Leal L</pubmed_authors><pubmed_authors>Ugarte A</pubmed_authors><pubmed_authors>Torres B</pubmed_authors><pubmed_authors>Fernandez M</pubmed_authors><pubmed_authors>Herrera S</pubmed_authors><pubmed_authors>Alvarez M</pubmed_authors><pubmed_authors>Foncillas A</pubmed_authors><pubmed_authors>Morata L</pubmed_authors><pubmed_authors>Rodriguez-Nunez O</pubmed_authors><pubmed_authors>Cardozo C</pubmed_authors><pubmed_authors>Duenas G</pubmed_authors><pubmed_authors>Inciarte A</pubmed_authors><pubmed_authors>Zamora-Martinez C</pubmed_authors><pubmed_authors>Tome A</pubmed_authors><pubmed_authors>Prieto-Gonzalez S</pubmed_authors><pubmed_authors>de la Mora L</pubmed_authors><pubmed_authors>Grau B</pubmed_authors><pubmed_authors>Grafia I</pubmed_authors><pubmed_authors>Moreno P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effects of Siltuximab Versus Corticosteroids in Preventing COVID-19 Pneumonia Disease Progression: Multicentre, Open-Label, Randomized Clinical Trial.</name><description>In 2020, COVID-19 caused a global health crisis, prompting research efforts and accelerating drug development. As part of this response, we conducted a phase 2b, multicentre, open-label, randomized (1:1) clinical trial to compare the effects of siltuximab versus corticosteroids on disease progression in hospitalized adults with COVID-19 pneumonia. Between April 2020 and January 2021, 82 patients were randomized to receive siltuximab and 80 corticosteroids (20 methylprednisolone and 60 dexamethasone). Median (IQR) age was 61 years (50-72). Nineteen patients allocated to siltuximab were admitted to the intensive care unit compared to eight receiving corticosteroids (p = 0.025). Corticosteroid treatment was independently associated with a higher risk of avoiding intensive care unit admission </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-15T09:07:12.961Z</modification><creation>2026-07-02T03:08:46.557Z</creation></dates><accession>S-EPMC12874496</accession><cross_references><pubmed>41641848</pubmed><doi>10.1111/cts.70491</doi></cross_references></HashMap>