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Convalescent Plasma for COVID-19: A multicenter, randomized clinical trial

Authors :
Itziar Arrieta-Aldea
Carolina Villegas
Ana Fernández-Cruz
Maria Liz Paciello
Isabel Saez-Serrano
Concepción Payares-Herrera
Ascension Ramos-Garrido
Mikel Mancheño-Losa
Cristina Avendaño-Solá
Javier García-Pérez
Mayte Pérez-Olmeda
Alba Bosch
Alejandro Callejas-Díaz
Maria del Castillo Jarilla-Fernandez
José Luis Bueno
Enric Contreras
José Alcamí
Jorge Calderon
Irene Romera
Jaime Lora-Tamayo
Ferran Torres
Elena Múñez-Rubio
Isabel Salcedo
Maria Lourdes Porras-Leal
Inmaculada Casas-Flecha
Belén Ruiz-Antorán
Jose Antonio Moreno-Chulilla
Jose Ramon Pano-Pardo
Maria Elena Madrigal
Eduard Muniz-Diaz
Jose Maria Domingo-Morera
Antonio Ramos-Martínez
Moncef Belhassen-García
Rosa Malo de Molina
Lydia Blanco
Rafael F. Duarte
Vicente Estrada
Olga Lopez-Villar
Instituto de Salud Carlos III - ISCIII
European Regional Development Fund (ERDF/FEDER)
Source :
Repisalud, Instituto de Salud Carlos III (ISCIII), Universitat Autònoma de Barcelona
Publication Year :
2020
Publisher :
Cold Spring Harbor Laboratory, 2020.

Abstract

Background: Passive immunotherapy with convalescent plasma (CP) is a potential treatment for COVID-19 for which evidence from controlled clinical trials is lacking. Methods: We conducted a multi-center, randomized clinical trial in patients hospitalized for COVID-19. All patients received standard of care treatment, including off-label use of marketed medicines, and were randomized 1:1 to receive one dose (250-300 mL) of CP from donors with IgG anti-SARS-CoV-2. The primary endpoint was the proportion of patients in categories 5, 6 or 7 of the COVID-19 ordinal scale at day 15. Results: The trial was stopped after first interim analysis due to the fall in recruitment related to pandemic control. With 81 patients randomized, there were no patients progressing to mechanical ventilation or death among the 38 patients assigned to receive plasma (0%) versus 6 out of 43 patients (14%) progressing in control arm. Mortality rates were 0% vs 9.3% at days 15 and 29 for the active and control groups, respectively. No significant differences were found in secondary endpoints. At inclusion, patients had a median time of 8 days (IQR, 6-9) of symptoms and 49,4% of them were positive for anti-SARS-CoV-2 IgG antibodies. Conclusions: Convalescent plasma could be superior to standard of care in avoiding progression to mechanical ventilation or death in hospitalized patients with COVID-19. The strong dependence of results on a limited number of events in the control group prevents drawing firm conclusions about CP efficacy from this trial. (Funded by Instituto de Salud Carlos III; NCT04345523). This research is funded by the Government of Spain, Ministry of Science and Innovation, Instituto de Salud Carlos III, grant number COV20/00072 (Royal Decree-Law 8/2020, of 17 March, on urgent extraordinary measures to deal with the economic and social impact of COVID-19), co-financed by the European Regional Development Fund (FEDER) ‘‘A way to make Europe’’ and supported by SCReN (Spanish Clinical Research Network), ISCIII, project PT17/0017/0009. Clinical trial insurance coverage was kindly donated by MARCH RS Correduría de Seguros y Reaseguros. Mikel Mancheño-Losa holds a "Río Hortega" research contract (expte. CM19/00226 No

Details

Database :
OpenAIRE
Journal :
Repisalud, Instituto de Salud Carlos III (ISCIII), Universitat Autònoma de Barcelona
Accession number :
edsair.doi.dedup.....e40af9897bc091f3f01f294640f5881a