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Pharmaceutical Statistics|September 30, 2011
Indirect comparisons in the comparative efficacy and non-inferiority settingsSteven Snapinn, Qi JiangPharmaceutical Statistics|February 17, 2012
An evaluation of methods for testing hypotheses relating to two endpoints in a single clinical trialTing-Li Su, Ekkehard Glimm, John Whitehead, et al.Pharmaceutical Statistics|February 17, 2012
A practical comparison of blinded methods for sample size reviews in survival data clinical trialsSusan Todd, Elsa Valdés-Márquez, Jodie WestPharmaceutical Statistics|March 21, 2012
The effect of variability and carryover on average bioequivalence assessment: a simulation studyMaría Pilar O Sánchez, Jordi Ocaña, Josep L CarrascoPharmaceutical Statistics|December 14, 2011
Viewpoint: observations on scaled average bioequivalenceScott D Patterson, Byron JonesPharmaceutical Statistics|December 14, 2011
Curtailed two-stage designs with two dependent binary endpointsChia-Min Chen, Yunchan ChiPharmaceutical Statistics|April 17, 2012
Establishing consistency across all regions in a multi-regional clinical trialHsiao-Hui Tsou, H M James Hung, Yue-Ming Chen, et al.Pharmaceutical Statistics|February 14, 2012
Type I error rate control in adaptive designs for confirmatory clinical trials with treatment selection at interimMartin Posch, Willi Maurer, Frank BretzPharmaceutical Statistics|February 14, 2012
A flexible multi-stage design for phase II oncology trialsMing T Tan, Xiaoping XiongPharmaceutical Statistics|December 6, 2011
Why a Bayesian approach to safety analysis in pharmacovigilance is importantDavid Prieto-Merino, George Quartey, Jixian Wang, et al.Pageof 120