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Contemporary Clinical Trials|April 30, 2017
Optimal adaptive group sequential design with flexible timing of sample size determinationLu Cui, Lanju Zhang, Bo YangStatistics in Medicine|March 22, 2016
Optimal flexible sample size design with robust powerLanju Zhang, Lu Cui, Bo YangContemporary Clinical Trials|March 10, 2015
Enrichment design with patient population augmentationBo Yang, Yijie Zhou, Lanju Zhang, et al.Journal of Biopharmaceutical Statistics|June 18, 2016
Regional efficacy assessment in multiregional clinical developmentYijie Zhou, Lu Cui, Bo Yang, et al.Statistics in Medicine|November 20, 2018
On the efficiency of adaptive sample size designLu Cui, Lanju ZhangValue in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|August 17, 2014
Two approaches to incorporate clinical data uncertainty into multiple criteria decision analysis for benefit-risk assessment of medicinal productsShihua Wen, Lanju Zhang, Bo YangStatistical Methods in Medical Research|January 18, 2021
An automation-based adaptive seamless design for dose selection and confirmation with improved power and efficiencyLu Cui, Tianyu Zhan, Lanju Zhang, et al.Statistics in Medicine|June 10, 2021
A practical response adaptive block randomization (RABR) design with analytic type I error protectionTianyu Zhan, Lu Cui, Ziqian Geng, et al.Journal of Biopharmaceutical Statistics|June 14, 2014
A note on breast cancer trials with pCR-based accelerated approvalYi Xia, Lu Cui, Bo YangJournal of Biopharmaceutical Statistics|October 31, 2014
One- and two-stage Arrhenius models for pharmaceutical shelf life predictionZhewen Fan, Lanju ZhangPageof 749