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Backfilling cohorts in phase I dose-escalation studies.

Helen Yvette BarnettOliver BoixDimitris KontosThomas F Jaki
Published in: Clinical trials (London, England) (2023)
Backfilling in phase I dose-escalation studies can substantially increase the accuracy of estimation of the maximum tolerated dose, with a larger impact in the setting with a dose-limiting toxicity event assessment period of only one cycle. This increased accuracy and reduction in the trial duration are at the cost of increased sample size.
Keyphrases
  • clinical trial
  • oxidative stress
  • randomized controlled trial
  • phase ii
  • placebo controlled