JSM 2012 Online Program

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298 *	Tue, 7/31/2012, 8:30 AM - 10:30 AM	CC-Room 27A
Advances in Bayesian Clinical Trial Design — Contributed Papers
Biopharmaceutical Section , International Chinese Statistical Association
Chair(s): Scott Miller, FDA
8:35 AM	A Bayesian Adaptive Randomization Design Using Placebo and Active Control — Yili Pritchett, Abbott Laboratories ; Qi Tang, Abbott Laboratories ; Kristine Broglio, Berry Consultants ; Weining Robieson, Abbott Laboratories ; Scott Berry, Berry Consultants
8:50 AM	A Spline-Based Hierarchical Model for Estimating Blood Glucose Profiles from CGM Data — Hui Zheng, Harvard Medical School ; David A Schoenfeld, Harvard Medical School
9:05 AM	Bayesian Adaptive Phase II Screening Design for Combination Trials — Chunyan Cai, MD Anderson Cancer Center ; Ying Yuan, MD Anderson Cancer Center ; Valen E Johnson, MD Anderson Cancer Center
9:20 AM	On Bayesian Design and Analysis for Trials with Multiple Primary Endpoints — Kimberly Crimin, Novartis ;
9:35 AM	Bayesian modeling of crossover studies of rare diseases including escape phase — Lili Ding, Cincinnati Children's Hospital Medical Center ; Yongchao Liu, University of Cincinnati ; Bin Huang, Cincinnati Children's Hospital Medical Center
9:50 AM	A Hybrid Bayesian/Frequentist Two-Stage Randomized Phase II Design — Dawn Peters, Oregon Health and Science University
10:05 AM	A Bayesian Response-Based Adaptive Randomization Design for Phase II Trials of Targeted Therapy — Yiyi Chen, Oregon Health and Science University ; Zunqiu Chen, Oregon Health and Science University ; Motomi Mori, Oregon Health and Science University ; Byung Park, Oregon Health and Science University ; Jeffrey W Tyner, Oregon Health and Science University ; Marc M Loriaux, Oregon Health and Science University ; Tibor Kovacsovics, Oregon Health and Science University ; Brian J Druker, Oregon Health and Science University

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