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                  <mods:namePart>Varona, Jose F.</mods:namePart>
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                  <mods:namePart>Landete, Pedro</mods:namePart>
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                  <mods:namePart>Paredes, Roger</mods:namePart>
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                  <mods:namePart>Vates, Roberto</mods:namePart>
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                  <mods:namePart>Torralba, Miguel</mods:namePart>
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                  <mods:namePart>Guisado-Vasco, Pablo</mods:namePart>
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                  <mods:namePart>Porras, Lourdes</mods:namePart>
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                  <mods:namePart>Ancochea, Julio</mods:namePart>
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                  <mods:namePart>Saiz, Elena</mods:namePart>
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                  <mods:namePart>Meira, Fernanda</mods:namePart>
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                  <mods:namePart>Jimeno, Jose M..</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Lopez-Martin, Jose A.</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Estrada, Vicente</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Universitat Autònoma de Barcelona</mods:namePart>
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                  <mods:dateIssued encoding="iso8601">2023</mods:dateIssued>
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               <mods:abstract>The APLICOV-PC study assessed the safety and preliminary efficacy of plitidepsin in hospitalized adult patients with COVID-19. In this follow-up study (E-APLICOV), the incidence of post-COVID-19 morbidity was evaluated and any long-term complications were characterized. Between January 18 and March 16, 2022, 34 of the 45 adult patients who received therapy with plitidepsin in the APLICOV-PC study were enrolled in E-APLICOV (median time from plitidepsin first dose to E-APLICOV enrollment, 16.8 months [range, 15.2-19.5 months]). All patients were functionally autonomous with regard to daily living (Barthel index: 100) and had normal physical examinations. From the APLICOV-PC date of discharge to the date of the extension visit, neither Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5) grade 3-4 complications nor QT prolongation or significant electrocardiogram (EKG) abnormalities were reported. Five (14.7%) patients had another COVID-19 episode after initial discharge from APLICOV-PC, and in 2 patients (5.9%), previously unreported chest X-ray findings were documented. Spirometry and lung-diffusion tests were normal in 29 (85.3%) and 27 (79.4%) patients, respectively, and 3 patients needed additional oxygen supplementation after initial hospital discharge. None of these patients required subsequent hospital readmission for disease-related complications. In conclusion, plitidepsin has demonstrated a favorable long-term safety profile in adult patients hospitalized for COVID-19. With the constraints of a low sample size and a lack of control, the rate of post-COVID-19 complications after treatment with plitidepsin is in the low range of published reports. (ClinicalTrials.gov Identifier: NCT05121740;).</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by/4.0/</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Plitidepsin</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>COVID-19</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>SARS-CoV-2</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Long COVID</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Post-COVID-19 complications</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Plitidepsin in adult patients with COVID-19 requiring hospital admission : A long-term follow-up analysis</mods:title>
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