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16 * | Sun, 8/9/2015, 2:00 PM - 3:50 PM | CC-611 | |
Exploring Bayesian Approaches in Drug Clinical Trials — Topic Contributed Papers | |||
Biopharmaceutical Section , Section on Bayesian Statistical Science , International Society for Bayesian Analysis (ISBA) , International Chinese Statistical Association , Biometrics Section | |||
Organizer(s): Freda Cooner, FDA/CDER | |||
Chair(s): Kathleen Fritsch, FDA | |||
2:05 PM | Bayesian Adaptive Commensurate Prior Methods for Rare Disease and Pediatric Clinical Trials — Bradley P. Carlin, University of Minnesota ; Cynthia Basu, University of Minnesota ; Brian Hobbs, MD Anderson Cancer Center | ||
2:25 PM | The Role of Simulation in Designing Rare Disease Trials — Jason Connor, Berry Consultants | ||
2:45 PM | Bayesian Approaches for Benefit-Risk Assessment — Ram Tiwari, FDA/CDER/OT/OB | ||
3:05 PM | Bayesian Opportunities in Clinical Trials from an Industry Perspective — Fanni Natanegara, Eli Lilly and Company ; Karen Price, Eli Lilly and Company | ||
3:25 PM | Discussant: Freda Cooner, FDA/CDER | ||
3:45 PM | Floor Discussion |
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