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dc.contributor.authorLandete, Pedro
dc.contributor.authorCaliman Sturdza, Olga Adriana e
dc.contributor.authorLopez Martin, Jose
dc.contributor.authorPreotescu, Liliana
dc.contributor.authorLuca, Mihaela Catalina
dc.contributor.authorKotanidou, Anastasia
dc.contributor.authorVillares, Paula
dc.contributor.authorIglesias, Shirley Patricia
dc.contributor.authorGuisado Vasco, Pablo
dc.contributor.authorSaiz Lou, Elena-Maria
dc.contributor.authorFariñas Álvarez, María del Carmen 
dc.contributor.authorDe Lucas, Esperanza Merino
dc.contributor.authorPerez Alba, Eduardo
dc.contributor.authorCisneros, Jose Miguel
dc.contributor.authorHidalgoTenorio, Carmen
dc.contributor.authorPoulakou, Garyfallia
dc.contributor.authorTorralba, Miguel
dc.contributor.authorFortun, Jesus
dc.contributor.authorGarcia Ocana, Paula
dc.contributor.authorLemaignen, Adrien
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-03-06T12:50:02Z
dc.date.available2025-03-06T12:50:02Z
dc.date.issued2024
dc.identifier.issn1058-4838
dc.identifier.issn1537-6591
dc.identifier.urihttps://hdl.handle.net/10902/35912
dc.description.abstractBackground: Plitidepsin has shown potent preclinical activity against severe acute respiratory syndrome coronavirus 2 and was generally well tolerated in a phase I trial of hospitalized patients with coronavirus disease 2019 (COVID-19). NEPTUNO, a phase III, multicenter, randomized, controlled trial, was designed to evaluate the efficacy and safety of plitidepsin in the management of moderate COVID-19 in hospitalized adult patients. Methods: Included patients had documented severe acute respiratory syndrome coronavirus 2 infection, required oxygen therapy, and had adequate organ function. The planned sample size was 609 patients. Patients were randomized 1:1:1 to at least 3 days of dexamethasone plus either plitidepsin (1.5 mg/day or 2.5 mg/day, for 3 days) or standard of care (control). The primary endpoint was the time to sustained withdrawal of supplemental oxygen. Secondary endpoints included time to sustained hospital discharge, clinical status, duration of oxygen support, percentage of patients requiring admission to the intensive care unit, and safety. Results: After randomizing 205 patients, NEPTUNO was discontinued due to a notable drop in COVID-19-related hospitalizations. Available data suggest a 2-day improvement in the median time to sustained oxygen therapy discontinuation (5 vs 7 days) favoring both plitidepsin arms (hazard ratio, 1.37; 95% confidence interval, .96-1.96; P = .08 for plitidepsin 1.5 mg vs control; hazard ratio, 1.06; 95% confidence interval, .73-1.53; P = .78 for plitidepsin 2.5 mg vs control). Plitidepsin was generally well tolerated. Conclusions: Despite the trial limitations, these results suggest that plitidepsin may have a positive benefit-risk ratio in the management of patients requiring oxygen therapy. Further studies with plitidepsin, including those in immunosuppressed patients, are warranted.Results from this phase III trial suggest that plitidepsin, a first-in-class antiviral, may have a positive benefit-risk ratio in the management of hospitalized patients requiring oxygen therapy for moderate COVID-19.es_ES
dc.description.sponsorshipThis work was supported by PharmaMar SA. (Colmenar Viejo, Spain). Financial support was intended to cover costs derived from the studyes_ES
dc.format.extent10 p.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.rights© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attributiones_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceClinical Infectious Diseases, 2024, 79(4), 910-919es_ES
dc.subject.otherPlitidepsines_ES
dc.subject.otherSARS-CoV-2es_ES
dc.subject.otherCOVID-19es_ES
dc.subject.otherAntiviral agentses_ES
dc.subject.otherMarine compoundses_ES
dc.titleA phase III randomized controlled trial of plitidepsin, a marine-derived compound, in hospitalized adults with moderate COVID-19es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1093/cid/ciae227es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1093/cid/ciae227
dc.type.versionpublishedVersiones_ES


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© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons AttributionExcepto si se señala otra cosa, la licencia del ítem se describe como © The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution