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Journal of Biopharmaceutical Statistics|October 21, 2017
A Bayesian Meta-analysis Method for Estimating Risk Difference of Rare EventsYuanyuan Tang, Qi Tang, Yao Yu, et al.
Journal of Biopharmaceutical Statistics|October 10, 2017
Statistical planning in confirmatory clinical trials with multiple treatment groups, multiple visits, and multiple endpointsHengrui Sun, Ellen Snyder, Gary G Koch
Journal of Biopharmaceutical Statistics|September 7, 2017
New designs for basket clinical trials in oncologyRichard Simon
Journal of Biopharmaceutical Statistics|April 5, 2017
Design of experiment for nonlinear dynamic gene regulatory network identificationTao Lu
Journal of Biopharmaceutical Statistics|February 7, 2017
An evaluation of increasing sample size based on conditional powerMichael Gaffney, James H Ware
Journal of Biopharmaceutical Statistics|September 12, 2019
Adaptive clinical endpoint bioequivalence studies with sample size re-estimation based on a nuisance parameterLin Zhu, Wanjie Sun
Journal of Biopharmaceutical Statistics|September 19, 2019
Propensity score-integrated power prior approach for incorporating real-world evidence in single-arm clinical studiesChenguang Wang, Heng Li, Wei-Chen Chen, et al.
Journal of Biopharmaceutical Statistics|February 15, 2019
Simulation optimization for Bayesian multi-arm multi-stage clinical trial with binary endpointsZhenning Yu, Viswanathan Ramakrishnan, Caitlyn Meinzer
Journal of Biopharmaceutical Statistics|March 14, 2017
Unified additional requirement in consideration of regional approval for multiregional clinical trialsZhaoyang Teng, Yeh-Fong Chen, Mark Chang
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