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Activity Details

486 Wed, 8/7/2013, 8:30 AM - 10:20 AM CC-510c
Adaptive Designs: Challenges of Design and Analysis — Contributed Papers
Biopharmaceutical Section , Biometrics Section
Chair(s): Grace Liu, Jansen Research Development
8:35 AM Inference from Blinded Data in Randomized Clinical Trials Kefei Zhou, Amgen. Co ; Jeetu Ganju, Gilead
8:50 AM Interim Analysis for the Mean Difference of Two Samples Using Generalized P-Values Richard McNally, Covance
9:05 AM Sequential Monitoring of Covariate Adaptive Designs Hongjian Zhu, The University of Texas Health Science Center at Houston ; Feifang Hu, University of Virginia
9:20 AM Adaptive Blinded Bayesian Sample Size Re-Determination for Clinical Trials: Extensions and Risk Minimizations Andrew Hartley, PPD, Inc
9:35 AM Small-Scale Studies and Their Impact on Phase III Trials: Vanguards, Pilot Studies, and Run-Ins Sarah Baraniuk, UT-School of Public Health
9:50 AM Testing Key Secondary Claims in Adaptive Design Settings George Kordzakhia, Food & Drug Administration ; Eiji Ishida, FDA ; John Lawrence, FDA
10:05 AM Testing Multiple Endpoints in Group Sequential Designs Guohui Liu, Millennium: The Takeda Oncology Company ; Yi Liu, Millennium : The Takeda Oncology Company

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