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145 Mon, 8/8/2022, 10:30 AM - 12:20 PM CC-140B
Leveraging External Data in Clinical Trials — Contributed Papers
Biopharmaceutical Section
Chair(s): Chris Holland, ImmunoCore
10:35 AM BOREC: A Bayesian Optimal Design for Randomized Dose Expansion Cohorts in Oncology Trials
Jinjie Chen, BMS; Rong Liu, BMS; Ruitao Lin, MD Anderson
10:50 AM Can Borrowing Historical Data Help? a Progression-Free Survival Data Analysis for Randomized Trial
Arnab Kumar Maity, Pfizer; Lada Aleksandrovna Markovtsova, Pfizer; Satrajit Roychoudhury, Pfizer Inc
11:05 AM A Matching Design for Augmenting a Randomized Clinical Trial with External Control
Jianghao Li, Eli Lilly and Company; Yu Du, Eli Lilly and Company; Yanyao Yi, Eli Lilly and Company; Huayu Liu, Eli Lilly and Company
11:20 AM Evaluating Propensity-Score Augmentation of Real-World Controls in Clinical Studies
Mingyang Shan, Eli Lilly and Company; Yang Ou, University of Pittsburgh; Tongrong Wang, Eli Lilly and Company; Ilya Lipkovich, Eli Lilly and Company; Douglas Faries, Eli Lilly & Company
11:35 AM Dynamic Regularized Bayes Borrowing Leveraging Efficiency of Estimation
Mohamad Hasan, Johnson & Johnson; Kate Stromberg, Janssen R&D, LLC
11:50 AM BPAD: A Bayesian Basket Design for Pediatric Trials with Adult Data
Yimei Li, University of Pennsylvania; Ying Yuan , the University of Texas MD Anderson Cancer Center
12:05 PM Leveraging Information from Historical Trials: A Case Study in Pediatric Multiple Sclerosis
Min Zhu, Bristol Myers Squibb; David Stivers, Bristol Myers Squibb; Judy Li, Bristol Myers Squibb