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Journal of Biopharmaceutical Statistics|February 27, 2013
An equivalence test for the comparison between a test drug and placebo in human abuse potential studiesLing Chen, Katherine R BonsonJournal of Biopharmaceutical Statistics|February 27, 2013
A more powerful test based on ratio distribution for retention noninferiority hypothesisLing Deng, Gang ChenJournal of Biopharmaceutical Statistics|February 27, 2013
The type II error probability of a group sequential test of efficacy and futility, and considerations for power and sample sizeThomas W DobbinsJournal of Biopharmaceutical Statistics|February 27, 2013
Estimating covariate-adjusted log hazard ratios in randomized clinical trials using cox proportional hazards models and nonparametric randomization based analysis of covarianceBenjamin R Saville, Gary G KochJournal of Biopharmaceutical Statistics|June 22, 2013
Estimation of the common risk difference in stratified paired binary data with homogeneous stratum effectYan D Zhao, Dewi RahardjaJournal of Biopharmaceutical Statistics|June 22, 2013
Detecting potential safety issues in large clinical or observational trials by Bayesian screening when event counts arise from poisson distributionsA Lawrence GouldJournal of Biopharmaceutical Statistics|June 22, 2013
Evaluating the performance of the ICH guidelines for shelf life estimationMichelle Quinlan, Walter Stroup, James Schwenke, et al.Journal of Biopharmaceutical Statistics|June 22, 2013
Medical records-based postmarketing safety evaluation of rare events with uncertain statusHongyuan Cao, Lisa M LaVange, Joseph F Heyse, et al.Journal of Biopharmaceutical Statistics|June 27, 2013
Three-arm noninferiority trials with a prespecified margin for inference of the difference in the proportions of binary endpointsEisuke Hida, Toshiro TangoJournal of Biopharmaceutical Statistics|August 21, 2013
Optimal timing for interim analyses in clinical trialsKanae Togo, Manabu IwasakiPageof 218