Bayesian methods for setting sample sizes and choosing allocation ratios in phase II clinical trials with time-to-event endpoints
Author:
Affiliation:
1. Medical and Pharmaceutical Statistics Research Unit, Department of Mathematics and Statistics; Lancaster University; Lancaster U.K.
Funder
National Institute for Health Research
Publisher
Wiley
Subject
Statistics and Probability,Epidemiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/sim.6426/fullpdf
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