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Pharmaceutical Statistics|March 20, 2013
Blinded sample size re-estimation in superiority and noninferiority trials: bias versus variance in variance estimationTim Friede, Meinhard KieserPharmaceutical Statistics|April 30, 2013
An efficient analysis of covariance model for crossover thorough QT studies with period-specific baseline daysKaifeng LuPharmaceutical Statistics|October 10, 2014
A note regarding meta-analysis of sequential trials with stopping for efficacyStephen SennPharmaceutical Statistics|November 30, 2012
A structured framework for assessing sensitivity to missing data assumptions in longitudinal clinical trialsC H Mallinckrodt, Q Lin, M MolenberghsPharmaceutical Statistics|October 17, 2014
Control of type 1 error in a hybrid complete two-period vaccine efficacy trialAndrew J Dunning, John ReevesPharmaceutical Statistics|April 19, 2026
A Dose-Finding Design for Drug Combinations Using a Bayesian 4 Parameter Logistic Model With Penalised D-OptimalityMaxine Ajimi, Benjamin Webb, Graham M Wheeler, et al.Pharmaceutical Statistics|April 19, 2026
Integrating Preclinical Insights for Adaptive Dose Escalation in Phase I Oncology TrialsHelen Barnett, Melanie Guhl, Fulvio Di Stefano, et al.Pharmaceutical Statistics|February 10, 2010
Statistical resource needs to be increased in the European regulatory agenciesOliver N Keene, Sara H Hughes, Nigel Howitt, et al.Pharmaceutical Statistics|June 15, 2007
The construction of multi-factor crossover designs in animal husbandry studiesS T Bate, J BoxallPharmaceutical Statistics|April 29, 2026
Predictive Biomarker Graphical Approach (PRIME) for Precision MedicineGina D'Angelo, Xiaowen Tian, Chuyu Deng, et al.Pageof 119