JSM 2012 Online Program

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493	Wed, 8/1/2012, 10:30 AM - 12:20 PM	CC-Room 25B
Bayesian Applications in Clinical Trial Safety Assessment — Topic Contributed Papers
Biopharmaceutical Section
Organizer(s): Haijun Ma, Amgen, Inc.
Chair(s): Haijun Ma, Amgen, Inc.
10:35 AM	Recent Developments of Bayesian Meta-Analysis for Safety Evaluation in Randomized Clinical Trials — Karen Price, Eli Lilly and Company
10:55 AM	Identifying Potential Adverse Events Dose-Response Relationships via Bayesian Indirect and Mixed Treatment Comparison Models — Haoda Fu ; Karen Price, Eli Lilly and Company ; Mary E. Nilsson, Eli Lilly and Company ; Stephen J. Ruberg, Eli Lilly and Company
11:15 AM	Bayesian Meta Experimental Design: Evaluating Cardiovascular Risk in New Antidiabetic Therapies to Treat Type 2 Diabetes — H. Xia, Amgen, Inc. ; Joseph Ibrahim, The University of North Carolina at Chapel Hill ; Ming-Hui Chen, University of Connecticut ; Thomas Liu, Amgen, Inc.
11:35 AM	Applications of Bayesian Model Selection for Clinical Safety Data — Bradley McEvoy, FDA/CDER ; Rajesh R Nandy, University of California at Los Angeles ; Ram C. Tiwari, FDA/CDER/OTS/OB
11:55 AM	Discussant: George Rochester, FDA
12:15 PM	Floor Discussion

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