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Journal of Biopharmaceutical Statistics|March 20, 2024
A Bayesian approach based on discounting factor for consistency assessment in multi-regional clinical trialLiang Tong, Chen Li, Jielai Xia, et al.Journal of Biopharmaceutical Statistics|March 29, 2024
Flexible seamless 2-in-1 design with sample size adaptationRunjia Li, Liwen Wu, Rachael Liu, et al.Journal of Biopharmaceutical Statistics|April 2, 2024
Optimization of EWOC principle in BLRM design for phase 1 oncology trialsXiaohan Guo, Sean Kent, Arnab Maity, et al.Journal of Biopharmaceutical Statistics|March 29, 2024
FDA experiences with a centralized statistical monitoring toolXiaofeng Tina Wang, Paul Schuette, Matilde KamJournal of Biopharmaceutical Statistics|April 5, 2024
An enriched approach to combining high-dimensional genomic and low-dimensional phenotypic dataJavier Cabrera, Birol Emir, Ge Cheng, et al.Journal of Biopharmaceutical Statistics|August 29, 2024
MOVER tests for non-inferiority of the difference between two binary-outcome treatments in the matched-pairs designLiangchang Xiu, Linlin Xie, Haiyi Yan, et al.Journal of Biopharmaceutical Statistics|October 30, 2024
Small sample adjustment for inference without assuming orthogonality in a mixed model for repeated measures analysisKazushi Maruo, Ryota Ishii, Yusuke Yamaguchi, et al.Journal of Biopharmaceutical Statistics|September 20, 2024
Developing large language models to detect adverse drug events in posts on xYu Deng, Yunzhao Xing, Jason Quach, et al.Journal of Biopharmaceutical Statistics|April 29, 2025
Application of complete N-of-1 trial design in bioequivalence-biosimilar drug developmentYuqing Liu, Wendy Lou, Shein-Chung ChowJournal of Biopharmaceutical Statistics|April 26, 2025
Comparison of continuous, binary, and ordinal endpointsJing Zhai, Fraser Smith, Guoxing SoonPageof 219