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Journal of Biopharmaceutical Statistics|February 26, 2010
Optimal two-stage designs allowing flexibility in number of subjects for phase II clinical trialsNobuyuki Masaki, Tatsuki Koyama, Isao Yoshimura, et al.Journal of Biopharmaceutical Statistics|February 26, 2010
Prediction of an outcome using trajectories estimated from a linear mixed modelNami Maruyama, Fumiaki Takahashi, Masahiro TakeuchiJournal of Biopharmaceutical Statistics|February 26, 2010
Data mining and statistically guided clinical review of adverse event data in clinical trialsH Southworth, M O'ConnellJournal of Biopharmaceutical Statistics|February 26, 2010
Sample size for testing difference between two proportions for the bilateral-sample designShi-Fang Qiu, Nian-Sheng Tang, Man-Lai Tang, et al.Journal of Biopharmaceutical Statistics|February 26, 2010
A Bayesian approach to evaluating regional treatment effect in a multiregional trialYi-Hau Chen, Ya-Chi Wu, Mey WangJournal of Biopharmaceutical Statistics|February 26, 2010
Increasing power in randomized trials with right censored outcomes through covariate adjustmentK L Moore, M J van der LaanJournal of Biopharmaceutical Statistics|September 27, 2016
Methods for efficacy evaluations of antibacterial treatments in multiple body-site infection trialsMohammad F Huque, Thamban Valappil, Mohamed Alosh, et al.Journal of Biopharmaceutical Statistics|June 19, 2018
A class of Covariate-Adjusted Response-Adaptive Allocation Designs for Multitreatment Binary Response TrialsAtanu Biswas, Rahul BhattacharyaJournal of Biopharmaceutical Statistics|August 11, 2018
Stochastic optimization of adaptive enrichment designs for two subpopulationsAaron Fisher, Michael Rosenblum, Journal of Biopharmaceutical Statistics|July 12, 2018
Estimation of causal effects in clinical endpoint bioequivalence studies in the presence of intercurrent events: noncompliance and missing dataYiyue Lou, Michael P Jones, Wanjie SunPageof 216