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259 ! | Mon, 8/10/2015, 2:00 PM - 3:50 PM | CC-613 | |
Clinical Trial Design II — Contributed Papers | |||
Biopharmaceutical Section , Biometrics Section | |||
Chair(s): Chia-Wen Ko, FDA | |||
2:05 PM | Doubly Robust Risk Estimation in the Presence of Informative Censoring Incorporating Time-Dependent Covariates — Takuya Kawahara, The University of Tokyo ; Yutaka Matsuyama, The University of Tokyo | ||
2:20 PM | Ignoring Site-Specific Treatment Effects in Multicenter Clinical Trials Increases False Positive Results — Eric Macklin, Massachusetts General Hospital/Harvard University | ||
2:35 PM | Influence of Prior on Bayesian Sample Size Calculation — Kevin Hou, Incyte Corporation ; Gongfu Zhou, Incyte Corporation ; Yufan Zhao, Incyte Corporation | ||
2:50 PM | Reference-Scaled Margin for Lot Consistency Study — Jin Xu, Merck ; G. Frank Liu, Merck | ||
3:05 PM | Multistage Adaptive Biomarker-Directed Targeted Clinical Trial Design — Zhong Gao, OBE/CBER/FDA ; Ming Tan, Georgetown University ; Anindya Roy, University of Maryland, Baltimore County | ||
3:20 PM | Assessing the Current and Potential Use of Adaptive Study Designs in Emergency Medicine Clinical Trials — Laura Flight, University of Sheffield ; Steven A. Julious, University of Sheffield ; Steve Goodacre, University of Sheffield | ||
3:35 PM | Identify Sources of Placebo Response Early to Improve the Probability of Success in Late-Stage Program — Weining Robieson, AbbVie ; Jun Zhao, AbbVie ; Deli Wang, AbbVie |
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