JSM 2015 Preliminary Program

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Legend: Washington State Convention Center = CC, Sheraton Seattle = S, Grand Hyatt = GH and The Conference Center = TCC
* = applied session       ! = JSM meeting theme

Activity Details
260 Mon, 8/10/2015, 2:00 PM - 3:50 PM CC-614
Missing Data II — Contributed Papers
Biopharmaceutical Section , Government Statistics Section
Chair(s): Rajesh Nair, FDA
2:05 PM A Two-Stage, Phase II Clinical Trial Design with Nested Criteria for Early Stopping and Efficacy — Daniel Zelterman, Yale University ; Michael Kane, Yale University ; Michelle DeVeaux, Yale University
2:20 PM Similarity Assessment of Chromatographic Fingerprint of Botanical Products — Xiaoyu Dong, FDA ; Yi Tsong, FDA ; Zhuang Miao, FDA ; Jinhui Dou, FDA
2:35 PM Improving Power for Biomarker Detection with Joint Modeling of Multiple Endpoints in Early-Phase Clinical Trials — Qianying Liu, Sanofi ; Glen Laird, Sanofi ; Wei Zheng, Sanofi
2:50 PM An Empirical Bayesian Approach to Bioequivalence Studies — Li He, Merck Research Laboratories ; Robert Capen, Merck Research Laboratories
3:05 PM Automated High-Dimensional Cytometry Analysis to Elucidate Phenotypic and Functional Modulation in Immuno Cellular Subpopulations — Shubing Wang, Merck ; An Chi, Merck ; Yujie Qu, Merck
3:20 PM Sample Size Calculation in Clinical Trials with Mixed Binary and Continuous Co-Primary Endpoints Modeled by Gaussian Copulas — Beilei Wu, PAREXEL International ; Alexander de Leon, University of Calgary ; Daniel Bonzo, PAREXEL International
3:35 PM Bayesian Prediction Model of Event Times in Randomized Clinical Trial — Jiang Li, Novartis ; Wentao Feng, Novartis ; Satrajit Roychoudhury, Novartis Pharmaceuticals




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