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Rethinking remdesivir for COVID-19: A Bayesian reanalysis of trial findings.

Joyce M HoekSarahanne M FieldYmkje Anna de VriesMaximilian LindeMerle-Marie PittelkowJasmine MuradchanianDon van Ravenzwaaij
Published in: PloS one (2021)
We recommend that regulatory bodies take all available evidence into account for endorsement decisions. A Bayesian approach can be beneficial, in particular in case of statistically non-significant results. This is especially pressing when limited clinical efficacy data is available.
Keyphrases
  • coronavirus disease
  • sars cov
  • study protocol
  • phase iii
  • electronic health record
  • clinical trial
  • transcription factor
  • phase ii
  • machine learning
  • data analysis
  • artificial intelligence