Sample size recalculation in three-stage clinical trials and its evaluation
Björn Bokelmann, Geraldine Rauch, Jan Meis, Meinhard Kieser, Carolin Herrmann

TL;DR
This paper explores how to adjust sample sizes in three-stage clinical trials and evaluates the benefits of such adjustments.
Contribution
The paper extends sample size recalculation methods to three-stage trials and evaluates their performance.
Findings
Three-stage designs show notable improvements in power and expected sample size compared to two-stage designs.
The benefits of recalculation depend on the performance measures and trial characteristics considered.
Recalculation rules can be applied in three-stage trials but their advantages are not always clear.
Abstract
In clinical trials, the determination of an adequate sample size is a challenging task, mainly due to the uncertainty about the value of the effect size and nuisance parameters. One method to deal with this uncertainty is a sample size recalculation. Thereby, an interim analysis is performed based on which the sample size for the remaining trial is adapted. With few exceptions, previous literature has only examined the potential of recalculation in two-stage trials. In our research, we address sample size recalculation in three-stage trials, i.e. trials with two pre-planned interim analyses. We show how recalculation rules from two-stage trials can be modified to be applicable to three-stage trials. We also illustrate how a performance measure, recently suggested for two-stage trial recalculation (the conditional performance score) can be applied to evaluate recalculation rules in…
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Taxonomy
TopicsStatistical Methods in Clinical Trials · Optimal Experimental Design Methods · Biosimilars and Bioanalytical Methods
