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Statistics in Medicine|March 27, 2015
Two-stage designs for cross-over bioequivalence trialsMeinhard Kieser, Geraldine Rauch
Journal of Biopharmaceutical Statistics|May 25, 2022
Two-stage designs with small sample sizesMeinhard Kieser, Geraldine Rauch, Maximilian Pilz
BMC Medical Research Methodology|February 7, 2020
Why do you need a biostatistician?Antonia Zapf, Geraldine Rauch, Meinhard Kieser
Journal of Biopharmaceutical Statistics|June 14, 2016
Blinded sample size recalculation in clinical trials with binary composite endpointsAnja Sander, Geraldine Rauch, Meinhard Kieser
BMC Medical Research Methodology|August 10, 2017
Choice of futility boundaries for group sequential designs with two endpointsSvenja Schüler, Meinhard Kieser, Geraldine Rauch
BMC Medical Research Methodology|January 6, 2018
A systematic comparison of recurrent event models for application to composite endpointsAnn-Kathrin Ozga, Meinhard Kieser, Geraldine Rauch
Pharmaceutical Statistics|May 23, 2022
Optimal unplanned design modification in adaptive two-stage trialsMaximilian Pilz, Carolin Herrmann, Geraldine Rauch, et al.
Biometrical Journal. Biometrische Zeitschrift|April 15, 2022
Optimization of adaptive designs with respect to a performance scoreCarolin Herrmann, Meinhard Kieser, Geraldine Rauch, et al.
World Journal of Cardiology|January 30, 2015
Opportunities and challenges of clinical trials in cardiology using composite primary endpointsGeraldine Rauch, Bernhard Rauch, Svenja Schüler, et al.
Statistics in Medicine|April 7, 2020
A new conditional performance score for the evaluation of adaptive group sequential designs with sample size recalculationCarolin Herrmann, Maximilian Pilz, Meinhard Kieser, et al.
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