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Journal of Biopharmaceutical Statistics|April 22, 2025
Double machine learning methods for estimating average treatment effects: a comparative studyXiaoqing Tan, Shu Yang, Wenyu Ye, et al.Journal of Biopharmaceutical Statistics|April 20, 2025
Biomarker-guided adaptive enrichment design with threshold detection for clinical trials with time-to-event outcomeKaiyuan Hua, Hwanhee Hong, Xiaofei WangJournal of Biopharmaceutical Statistics|April 30, 2025
A practical analysis procedure on generalizing comparative effectiveness in the randomized clinical trial to the real-world trial-eligible populationKuan Jiang, Xin-Xing Lai, Shu Yang, et al.Journal of Biopharmaceutical Statistics|April 20, 2025
Study duration prediction for clinical trials with time-to-event endpoints accounting for heterogeneous populationHong Zhang, Jie Pu, Shibing Deng, et al.Journal of Biopharmaceutical Statistics|November 13, 2025
Curtailed procedures for binomial random-sized subset selectionYifang Zhang, Pinyuen ChenJournal of Biopharmaceutical Statistics|November 11, 2025
Tables, listings and figures in a clinical study report - quality or quantity?Ning Li, Yaohua Zhang, Naitee TingJournal of Biopharmaceutical Statistics|December 5, 2025
Saddlepoint p-values for the class of bivariate two-sample tests under generalized randomized block designAbd El-Raheem M Abd El-Raheem, Ibrahim A A Shanan, Mona HosnyJournal of Biopharmaceutical Statistics|November 13, 2025
Power priors and type I error control: constrained borrowing of external control dataSe Yoon LeeJournal of Biopharmaceutical Statistics|July 18, 2014
Clinical development and trial design of biosimilar products: a Japanese perspectiveMasayuki Nagasaki, Yuki AndoJournal of Biopharmaceutical Statistics|July 19, 2014
Covariate effect on constancy assumption in noninferiority clinical trialsSiyan Xu, Kerry Barker, Sandeep Menon, et al.Pageof 218