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113 * ! Mon, 7/30/2012, 8:30 AM - 10:20 AM CC-Room 23A
Dose Selection in Clinical Trials — Topic Contributed Papers
Biopharmaceutical Section , International Indian Statistical Association
Organizer(s): Weihua Cao, FDA
Chair(s): zhi wen, FDA
8:35 AM Simultaneous Inference for Dose Selection with Binary Responses Bernhard Klingenberg, Williams College
8:55 AM Utility-Based Dose-Finding in Phase I-II Clinical Trials Peter Thall, MD Anderson Cancer Center ; Hoang Q Nguyen, MD Anderson Cancer Center
9:15 AM Characterizing Dose-Response in the Development of Novel Treatments for Multiple Sclerosis David I Ohlssen, Novartis
9:35 AM Designing Phase 2 Trials Based on Program-Level Criteria Nitin Patel, Cytel Inc. ; James Bolognese, Cytel Inc. ; Christy Chuang-Stein, Pfizer Inc. ; David Hewitt, Merck ; Arnold Gammaitoni, Nuvo Research ; Jose Carlos Pinheiro, Johnson & Johnson
9:55 AM Discussant: Amelia Dale Horne, FDA
10:15 AM Floor Discussion



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