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Pharmaceutical Statistics|December 6, 2011
Predictive event modelling in multicenter clinical trials with waiting time to responseVladimir V AnisimovPharmaceutical Statistics|March 13, 2012
Analysis of dose-response in flexible dose titration clinical studiesXu Steven Xu, Min Yuan, Partha NandyPharmaceutical Statistics|November 8, 2014
Effect of reporting bias in the analysis of spontaneous reporting dataPalash Ghosh, Anup DewanjiPharmaceutical Statistics|November 22, 2014
Validation of qualitative microbiological test methodsPieta C IJzerman-Boon, Edwin R van den HeuvelPharmaceutical Statistics|November 7, 2019
Coherence principles in interval-based dose findingNolan A Wages, Alexia Iasonos, John O'Quigley, et al.Pharmaceutical Statistics|December 13, 2019
Sequential parallel comparison design with two coprimary endpointsGosuke Homma, Takashi DaimonPharmaceutical Statistics|February 25, 2020
Designing cancer immunotherapy trials with delayed treatment effect using maximin efficiency robust statisticsXue Ding, Jianrong WuPharmaceutical Statistics|February 29, 2020
Estimation of group means using Bayesian generalized linear mixed modelsAmy LaLonde, Yongming QuPharmaceutical Statistics|March 22, 2020
Comparison of response adaptive randomization features in multiarm clinical trials with controlKert Viele, Benjamin R Saville, Anna McGlothlin, et al.Pharmaceutical Statistics|December 12, 2018
Propensity-score-based priors for Bayesian augmented control designJunjing Lin, Margaret Gamalo-Siebers, Ram TiwariPageof 120