4.6 Article

CATALYST trial protocol: a multicentre, open-label, phase II, multiarm trial for an early and accelerated evaluation of the potential treatments for COVID-19 in hospitalised adults

期刊

BMJ OPEN
卷 11, 期 11, 页码 -

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/bmjopen-2021-050202

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资金

  1. Medical Research Council (MRC) [MC_PC_20007]
  2. National Institute of Health Research
  3. Cancer Research UK [C22436/A25354]
  4. NIHR Biomedical Research Centre [BRC-1215-20009]
  5. Kennedy Trust for Rheumatology Research, Arthritis-Trials Acceleration Programme [KENN161704]
  6. Innovate UK, Midlands-Wales Advanced Therapy Treatment Centres [104232]
  7. NIHR Birmingham Biomedical Research Centres at the University Hospitals Birmingham NHS Foundation Trust
  8. Oxford and University College London Hospitals Biomedical Research Centres
  9. University of Birmingham
  10. MRC [MC_PC_20007] Funding Source: UKRI

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The CATALYST trial aims to identify novel treatments for COVID-19 patients through immunomodulation to improve outcomes. The trial has been approved by the appropriate ethics committee and will disseminate results through national and international presentations and peer-reviewed publications.
Introduction Severe SARS-CoV-2 infection is associated with a dysregulated immune response. Inflammatory monocytes and macrophages are crucial, promoting injurious, proinflammatory sequelae. Immunomodulation is, therefore, an attractive therapeutic strategy and we sought to test licensed and novel candidate drugs. Methods and analysis The CATALYST trial is a multiarm, open-label, multicentre, phase II platform trial designed to identify candidate novel treatments to improve outcomes of patients hospitalised with COVID-19 compared with usual care. Treatments with evidence of biomarker improvements will be put forward for larger-scale testing by current national phase Ill platform trials. Hospitalised patients >16 years with a clinical picture strongly suggestive of SARS-CoV-2 pneumonia (confirmed by chest X-ray or CT scan, with or without a positive reverse transcription PCR assay) and a C reactive protein (CRP) >= 40mg/L are eligible. The primary outcome measure is CRP, measured serially from admission to day 14, hospital discharge or death. Secondary outcomes include the WHO Clinical Progression Improvement Scale as a principal efficacy assessment. Ethics and dissemination The protocol was approved by the East Midlands-Nottingham 2 Research Ethics Committee (20/EM/0115) and given urgent public health status; initial approval was received on 5 May 2020, current protocol version (V.6.0) approval on 12 October 2020. The MHRA also approved all protocol versions. The results of this trial will be disseminated through national and international presentations and peer-reviewed publications.

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