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Pharmaceutical Statistics|March 19, 2021
Power and sample size for GEE analysis of incomplete paired outcomes in 2 × 2 crossover trialsYongqiang TangPharmaceutical Statistics|January 21, 2014
Balance and randomness in sequential clinical trials: the dominant biased coin designAlessandro Baldi Antognini, Maroussa ZagoraiouPharmaceutical Statistics|June 4, 2014
When is a seamless study desirable? Case studies from different pharmaceutical sponsorsRobert L Cuffe, David Lawrence, Andrew Stone, et al.Pharmaceutical Statistics|June 17, 2014
Subgroup analyses in cost-effectiveness analyses to support health technology assessmentsChristine Fletcher, Christy Chuang-Stein, Marie-Ange Paget, et al.Pharmaceutical Statistics|June 29, 2012
Attenuation of treatment effect due to measurement variability in assessment of progression-free survivalS Hong, N Schmitt, A Stone, et al.Pharmaceutical Statistics|August 14, 2012
Measurement error and outcomes defined by exceeding a threshold: biased findings in comparative effectiveness trialsPetra BůžkováPharmaceutical Statistics|August 14, 2012
Multivariate extreme value modelling of laboratory safety data from clinical studiesHarry Southworth, Janet E HeffernanPharmaceutical Statistics|February 4, 2015
Evaluation of program success for programs with multiple trials in binary outcomesMeihua Wang, G Frank Liu, Jerald SchindlerPharmaceutical Statistics|February 10, 2015
Modifications of sequential designs in bioequivalence trialsCheng Zheng, Lihui Zhao, Jixian WangPageof 120