Publication:
Remdesivir and three other drugs for hospitalised patients with COVID-19: final results of the WHO Solidarity randomised trial and updated meta-analyses.

cris.virtual.author-orcid0000-0002-8162-8910
cris.virtualsource.author-orcid41fcad6b-7148-4d79-b498-4c3b0e04dcf8
cris.virtualsource.author-orcid261c592a-cd6e-4c32-b0f7-ca6c7ff7e96a
cris.virtualsource.author-orcid321b355e-036e-464b-a409-b5f84db839cb
cris.virtualsource.author-orcid3b12b088-ef2b-4665-b7a5-265aa75ade43
datacite.rightsopen.access
dc.contributor.authorPan, Hongchao
dc.contributor.authorPeto, Richard
dc.contributor.authorHenao-Restrepo, Ana-Maria
dc.contributor.authorPreziosi, Marie-Pierre
dc.contributor.authorSathiyamoorthy, Vasee
dc.contributor.authorAbdool Karim, Quarraisha
dc.contributor.authorAlejandria, Marissa M
dc.contributor.authorHernández García, César
dc.contributor.authorKieny, Marie-Paule
dc.contributor.authorMalekzadeh, Reza
dc.contributor.authorMurthy, Srinivas
dc.contributor.authorReddy, K Srinath
dc.contributor.authorRoses Periago, Mirta
dc.contributor.authorAbi Hanna, Pierre
dc.contributor.authorAbutidze, Akaki
dc.contributor.authorAder, Florence
dc.contributor.authorAl-Bader, Abdullah M
dc.contributor.authorAlhasawi, Almonther
dc.contributor.authorAllum, Emma
dc.contributor.authorAl Mawali, Adhra
dc.contributor.authorAlotaibi, Athari
dc.contributor.authorAlvarez-Moreno, Carlos A
dc.contributor.authorAppadoo, Sheila
dc.contributor.authorArts, Derk
dc.contributor.authorAsiri, Abdullah
dc.contributor.authorAukrust, Pål
dc.contributor.authorBarratt-Due, Andreas
dc.contributor.authorBayih, Abebe Genetu
dc.contributor.authorBeaumont, Helena
dc.contributor.authorBellani, Samir
dc.contributor.authorBenassi, Virginia
dc.contributor.authorBhargava, Balram
dc.contributor.authorBranca, Mattia
dc.contributor.authorCappel-Porter, Heike B C
dc.contributor.authorCerrato, Nery
dc.contributor.authorCheick Haidara, Fadima
dc.contributor.authorChow, Ting S
dc.contributor.authorComo, Najada
dc.contributor.authorEustace, Joe
dc.contributor.authorGabunia, Tamar
dc.contributor.authorGarcía, Patricia J
dc.contributor.authorGodbole, Sheela
dc.contributor.authorGotuzzo, Eduardo
dc.contributor.authorGriskevicius, Laimonas
dc.contributor.authorHamra, Rasha
dc.contributor.authorHassan, Mariam
dc.contributor.authorHassany, Mohamed
dc.contributor.authorHutton, David
dc.contributor.authorIrmansyah, Irmansyah
dc.contributor.authorJancoriene, Ligita
dc.contributor.authorKhamis, Faryal
dc.contributor.authorKirwan, Jana
dc.contributor.authorKumar, Suresh
dc.contributor.authorLopardo, Gustavo
dc.contributor.authorLydon, Patrick
dc.contributor.authorMagrini, Nicola
dc.contributor.authorManevska, Suzana
dc.contributor.authorManuel, Oriol
dc.contributor.authorMcGinty, Sibylle
dc.contributor.authorMedina, Marco T
dc.contributor.authorMesa Rubio, María L
dc.contributor.authorMiranda-Montoya, Maria C
dc.contributor.authorNel, Jeremy
dc.contributor.authorNunes, Estevao P
dc.contributor.authorPerola, Markus
dc.contributor.authorPortolés, Antonio
dc.contributor.authorRasmin, Menaldi
dc.contributor.authorRaza, Aun
dc.contributor.authorRees, Helen
dc.contributor.authorReges, Paula
dc.contributor.authorRogers, Chris
dc.contributor.authorSalami, Kolawole
dc.contributor.authorSalvadori, Marina
dc.contributor.authorSauermann, Mamatha
dc.contributor.authorSinani, Narvina
dc.contributor.authorSow, Samba
dc.contributor.authorSterne, Jonathan A C
dc.contributor.authorStevanovikj, Milena
dc.contributor.authorTacconelli, Evelina
dc.contributor.authorTavares Maltez, Fernando Manuel
dc.contributor.authorTeferi, Mekonnen
dc.contributor.authorTikkinen, Kari
dc.contributor.authorTrelle, Sven
dc.contributor.authorTsertsvadze, Tengiz
dc.contributor.authorZaid, Hala
dc.contributor.authorRottingen, Arne
dc.contributor.authorSwaminathan, Soumya
dc.contributor.authorRyan, Michael
dc.date.accessioned2025-04-09T16:41:57Z
dc.date.available2025-04-09T16:41:57Z
dc.date.issued2022-05-21
dc.description.abstractBACKGROUND World Health Organization expert groups recommended mortality trials of four repurposed antiviral drugs - remdesivir, hydroxychloroquine, lopinavir, and interferon beta-1a - in patients hospitalized with coronavirus disease 2019 (Covid-19). METHODS We randomly assigned inpatients with Covid-19 equally between one of the trial drug regimens that was locally available and open control (up to five options, four active and the local standard of care). The intention-to-treat primary analyses examined in-hospital mortality in the four pairwise comparisons of each trial drug and its control (drug available but patient assigned to the same care without that drug). Rate ratios for death were calculated with stratification according to age and status regarding mechanical ventilation at trial entry. RESULTS At 405 hospitals in 30 countries, 11,330 adults underwent randomization; 2750 were assigned to receive remdesivir, 954 to hydroxychloroquine, 1411 to lopinavir (without interferon), 2063 to interferon (including 651 to interferon plus lopinavir), and 4088 to no trial drug. Adherence was 94 to 96% midway through treatment, with 2 to 6% crossover. In total, 1253 deaths were reported (median day of death, day 8; interquartile range, 4 to 14). The Kaplan-Meier 28-day mortality was 11.8% (39.0% if the patient was already receiving ventilation at randomization and 9.5% otherwise). Death occurred in 301 of 2743 patients receiving remdesivir and in 303 of 2708 receiving its control (rate ratio, 0.95; 95% confidence interval [CI], 0.81 to 1.11; P = 0.50), in 104 of 947 patients receiving hydroxychloroquine and in 84 of 906 receiving its control (rate ratio, 1.19; 95% CI, 0.89 to 1.59; P = 0.23), in 148 of 1399 patients receiving lopinavir and in 146 of 1372 receiving its control (rate ratio, 1.00; 95% CI, 0.79 to 1.25; P = 0.97), and in 243 of 2050 patients receiving interferon and in 216 of 2050 receiving its control (rate ratio, 1.16; 95% CI, 0.96 to 1.39; P = 0.11). No drug definitely reduced mortality, overall or in any subgroup, or reduced initiation of ventilation or hospitalization duration. CONCLUSIONS These remdesivir, hydroxychloroquine, lopinavir, and interferon regimens had little or no effect on hospitalized patients with Covid-19, as indicated by overall mortality, initiation of ventilation, and duration of hospital stay. (Funded by the World Health Organization; ISRCTN Registry number, ISRCTN83971151; ClinicalTrials.gov number, NCT04315948.).
dc.description.numberOfPages13
dc.description.sponsorshipDepartment of Clinical Research (DCR)
dc.description.sponsorshipDepartment of Clinical Research, Clinical Trials Unit Bern
dc.description.sponsorshipDepartment of Clinical Research (DCR) - Data Management CTU
dc.description.sponsorshipDepartment of Clinical Research (DCR) - Statistics & Methodology (Bütikofer)
dc.identifier.doi10.7892/boris.170196
dc.identifier.pmid35512728
dc.identifier.publisherDOI10.1016/S0140-6736(22)00519-0
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/209593
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofLancet
dc.relation.issn0140-6736
dc.relation.organizationDCD5A442BE42E17DE0405C82790C4DE2
dc.titleRemdesivir and three other drugs for hospitalised patients with COVID-19: final results of the WHO Solidarity randomised trial and updated meta-analyses.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
dspace.file.typetext
oaire.citation.endPage1953
oaire.citation.issue10339
oaire.citation.startPage1941
oaire.citation.volume399
oairecerif.author.affiliationDepartment of Clinical Research (DCR) - Data Management CTU
oairecerif.author.affiliationDepartment of Clinical Research (DCR) - Statistics & Methodology (Bütikofer)
oairecerif.author.affiliationDepartment of Clinical Research (DCR)
oairecerif.author.affiliationDepartment of Clinical Research, Clinical Trials Unit Bern
oairecerif.author.affiliation2Department of Clinical Research (DCR)
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.date.licenseChanged2022-05-23 17:20:22
unibe.description.ispublishedpub
unibe.eprints.legacyId170196
unibe.journal.abbrevTitleLANCET
unibe.refereedtrue
unibe.subtype.articlejournal

Files

Original bundle
Now showing 1 - 2 of 2
Name:
WHOSolidarityTrialConsortium_Lancet_2022.pdf
Size:
973.25 KB
Format:
Adobe Portable Document Format
File Type:
text
License:
https://creativecommons.org/licenses/by/4.0
Content:
published
Name:
WHOSolidarityTrialConsortium_Lancet_2022_supplmat.pdf
Size:
1.46 MB
Format:
Adobe Portable Document Format
File Type:
text
License:
https://creativecommons.org/licenses/by/4.0
Content:
supplemental

Collections