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Journal of Biopharmaceutical Statistics|February 16, 2024
Considerations for master protocols using external controlsJie Chen, Xiaoyun Nicole Li, Chengxing Cindy Lu, et al.Journal of Biopharmaceutical Statistics|February 9, 2024
Miettinen and Nurminen score statistics revisitedAntonio Martín Andrés, Francisco Gayá Moreno, María Álvarez Hernández, et al.Journal of Biopharmaceutical Statistics|March 19, 2024
On the use of RWD in support of regulatory submission in drug developmentShein-Chung Chow, Peijin WangJournal of Biopharmaceutical Statistics|March 22, 2024
Analysis of innovative two-stage seamless adaptive design with different endpoints and population shiftWeijia Mai, Shein-Chung ChowJournal of Biopharmaceutical Statistics|March 22, 2024
Incorporating external real-world data (RWD) in confirmatory adaptive designJunjing Lin, Jianchang LinJournal 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.Pageof 216