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Journal of Biopharmaceutical Statistics|March 29, 2023
A confirmatory basket design considering non-inferiority and superiority testingYaohua Zhang, Chenghao Chu, Robert A Beckman, et al.Journal of Biopharmaceutical Statistics|June 5, 2014
Power and sample size for randomized phase III survival trials under the Weibull modelJianrong WuJournal of Biopharmaceutical Statistics|May 27, 2015
Assessing the impact of safety monitoring on the efficacy analysis in large Phase III group sequential trials with non-trivial safety event rateYanqiu Weng, Yuko Y Palesch, Stacia M DeSantis, et al.Journal of Biopharmaceutical Statistics|March 20, 2023
Simple methods for comparing two predictive values with incomplete dataYougui WuJournal of Biopharmaceutical Statistics|March 23, 2023
Application of estimand framework in ICH E9 (R1) to safety evaluationXuelong Wang, Ping Yang, Shuai S Yuan, et al.Journal of Biopharmaceutical Statistics|January 30, 2023
Hybrid continuous reassessment method with overdose control for safer dose escalationDebopriya Ghosh, Hong Xie, Liangcai Zhang, et al.Journal of Biopharmaceutical Statistics|February 10, 2023
A Bayesian joint model for multivariate longitudinal and time-to-event data with application to ALL maintenance studiesDamitri Kundu, Partha Sarkar, Kiranmoy DasJournal of Biopharmaceutical Statistics|February 3, 2023
Response adaptive randomization design for a two-stage study with binary responseGuogen ShanJournal of Biopharmaceutical Statistics|February 6, 2023
Group sequential designs for cancer immunotherapy trial with delayed treatment effectJianrong Wu, Yimei Li, Liang ZhuJournal of Biopharmaceutical Statistics|September 6, 2012
Assessing dose-region profile of drug efficacy: a multiregional trial strategyYi-Hau Chen, Mey WangPageof 216