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Dimethyl fumarate in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial
- RECOVERY Collaborative Group; Peter W Horby; Leon Peto; Natalie Staplin; Mark Campbell; Guilherme Pessoa-Amorim; Marion Mafham; Jonathan R Emberson; Richard Stewart; Benjamin Prudon; Alison Uriel; Christopher A Green; Devesh J Dhasmana; Flora Malein; Jaydip Majumdar; Paul Collini; Jack Shurmer; Bryan Yates; J Kenneth Baillie; Maya H Buch; Jeremy N Day; Saul N Faust; Thomas Jaki; Katie Jeffery; Edmund Juszczak; Marian Knight; Wei Shen Lim; Alan Montgomery; Andrew Mumford; Kathryn Rowan; Guy Thwaites; Richard Haynes; Martin Landray.
Afiliação
  • - RECOVERY Collaborative Group;
  • Peter W Horby; Pandemic Sciences Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom
  • Leon Peto; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Natalie Staplin; MRC Population Health Research Unit, University of Oxford, Oxford, United Kingdom
  • Mark Campbell; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Guilherme Pessoa-Amorim; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Marion Mafham; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Jonathan R Emberson; MRC Population Health Research Unit, University of Oxford, Oxford, United Kingdom
  • Richard Stewart; Milton Keynes University Hospital NHS Foundation Trust
  • Benjamin Prudon; North Tees and Hartlepool NHS Foundation Trust
  • Alison Uriel; Manchester University NHS Foundation Trust
  • Christopher A Green; University Hospitals Birmingham NHS Foundation Trust
  • Devesh J Dhasmana; Victoria Hospital Kirkcaldy, NHS Fife
  • Flora Malein; Liverpool University Hospitals NHS Foundation Trust
  • Jaydip Majumdar; Mid Cheshire Hospitals NHS Foundation Trust
  • Paul Collini; Sheffield Teaching Hospitals NHS Foundation Trust
  • Jack Shurmer; Bolton NHS Foundation Trust
  • Bryan Yates; Northumbria Healthcare NHS Foundation Trust
  • J Kenneth Baillie; Roslin Institute, University of Edinburgh
  • Maya H Buch; Centre for Musculoskeletal Research, University of Manchester, Manchester, United Kingdom
  • Jeremy N Day; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
  • Saul N Faust; NIHR Southampton Clinical Research Facility and Biomedical Research Centre, University of Southampton, Southampton, United Kingdom
  • Thomas Jaki; University of Regensburg, Germany
  • Katie Jeffery; Oxford University Hospitals NHS Foundation Trust
  • Edmund Juszczak; School of Medicine, University of Nottingham, Nottingham, United Kingdom
  • Marian Knight; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
  • Wei Shen Lim; School of Medicine, University of Nottingham, Nottingham, United Kingdom
  • Alan Montgomery; School of Medicine, University of Nottingham, Nottingham, United Kingdom
  • Andrew Mumford; School of Cellular and Molecular Medicine, University of Bristol, Bristol, United Kingdom
  • Kathryn Rowan; Intensive Care National Audit & Research Centre, London, United Kingdom
  • Guy Thwaites; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam
  • Richard Haynes; MRC Population Health Research Unit, University of Oxford, Oxford, United Kingdom
  • Martin Landray; Nuffield Department of Population Health, University of Oxford, Oxford, United Kingdom
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22280285
ABSTRACT
BackgroundDimethyl fumarate (DMF) is an anti-inflammatory drug that has been proposed as a treatment for patients hospitalised with COVID-19 MethodsThis randomised, controlled, open-label platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), is assessing multiple possible treatments in patients hospitalised for COVID-19. In this initial assessment of DMF, performed at 27 UK hospitals, eligible and consenting adults were randomly allocated (11) to either usual standard of care alone or usual standard of care plus DMF 120mg twice daily for 2 days followed by 240mg twice daily for 8 days, or until discharge if sooner. The primary outcome was clinical status on day 5 measured on a seven-point ordinal scale, assessed using a proportional odds model. Secondary outcomes were time to sustained improvement in clinical status, time to discharge, day 5 peripheral blood oxygenation, day 5 C-reactive protein, and improvement in day 10 clinical status. The trial is registered with ISRCTN (50189673) and clinicaltrials.gov (NCT04381936). FindingsBetween 2 March 2021 and 18 November 2021, 713 patients were enrolled in the DMF evaluation, of whom 356 were randomly allocated to receive usual care plus DMF, and 357 to usual care alone. 95% of patients were receiving corticosteroids as part of routine care. There was no evidence of a beneficial effect of DMF on clinical status at day 5 (common odds ratio of unfavourable outcome 1.12; 95% CI 0.85-1.46; p=0.42). There was no significant effect of DMF on any secondary outcome. As expected, DMF caused flushing and gastrointestinal symptoms, each in around 6% of patients, but no new adverse effects were identified. InterpretationIn adults hospitalised with COVID-19, DMF was not associated with an improvement in clinical outcomes. FundingUK Research and Innovation (Medical Research Council) and National Institute of Health Research (Grant ref MC_PC_19056).
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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