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Discussion on "Predictively consistent prior effective sample sizes," by Beat Neuenschwander, Sebastian Weber, Heinz Schmidli, and Anthony O'Hagan.

Atanu BiswasJean-François Angers
Published in: Biometrics (2020)
We extend the approach of finding effective sample size for a typical phase II clinical trial having efficacy and toxicity as two components of the response vector. The case of binary efficacy and binary toxicity is illustrated under Dirichlet and multivariate T priors.
Keyphrases
  • phase ii
  • clinical trial
  • open label
  • oxidative stress
  • ionic liquid
  • phase iii
  • double blind
  • study protocol
  • placebo controlled
  • heart rate
  • blood pressure
  • data analysis