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Journal of Biopharmaceutical Statistics|December 23, 2021
Propensity score-integrated Bayesian prior approaches for augmented control designs: a simulation studyXi Wang, Leah Suttner, Thomas Jemielita, et al.Journal of Biopharmaceutical Statistics|September 19, 2022
Retrieved-Dropout-Based multiple imputation for time-to-event data in cardiovascular outcome trialsJiwei He, Roberto Crackel, William Koh, et al.Journal of Biopharmaceutical Statistics|January 5, 2022
Exploring the Potential of External Control Arms created from Patient Level Data: A case study in non-small cell lung cancerXiang Yin, Pallavi S Mishra-Kalyan, Rajeshwari Sridhara, et al.Journal of Biopharmaceutical Statistics|September 23, 2015
Statistical approaches for evaluating surrogate outcomes in clinical trials: A systematic reviewHannah Ensor, Robert J Lee, Cathie Sudlow, et al.Journal of Biopharmaceutical Statistics|November 6, 2014
Statistical assessment of biosimilarity based on the relative distance between follow-on biologics for binary endpointsWooyoung Shin, Seung-Ho KangJournal of Biopharmaceutical Statistics|September 15, 2015
Nine-year change in statistical design, profile, and success rates of Phase II oncology trialsAnastasia Ivanova, Barry Paul, Olga Marchenko, et al.Journal of Biopharmaceutical Statistics|September 16, 2015
Statistical innovations in the medical device world sparked by the FDAGregory Campbell, Lilly Q YueJournal of Biopharmaceutical Statistics|March 25, 2016
Sensitivity analyses for informative censoring in survival data: A trial exampleYanning LiuJournal of Biopharmaceutical Statistics|April 30, 2019
Robust designs in longitudinal studies accounting for parameter and model uncertainties - application to count dataFlorence Loingeville, Thu Thuy Nguyen, Marie-Karelle Riviere, et al.Journal of Biopharmaceutical Statistics|July 17, 2018
Confidence intervals for proportion ratios of stratified correlated bilateral dataTingting Zhuang, Guo-Liang Tian, Chang-Xing MaPageof 217