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Activity Details


72 * Sun, 8/3/2014, 4:00 PM - 5:50 PM CC-208
Biomarkers and Endpoint Validation 1 — Contributed Papers
Biopharmaceutical Section
Chair(s): Rajesh Nair,   
4:05 PM Filtering, Bias, and Biomarker Identification Gregory Hather, Takeda ; Ray Liu, Takeda
4:20 PM A Nonparametric Visualization Method to Measuring the Potential of Biomarkers for Guiding Treatment Decisions Hui Yang, Amgen ; Rui (Sammi) Tang, Amgen ; Michael Hale, Amgen ; Jing Huang, Amgen
4:35 PM Biomarker Signatures for Patient Subgroup Selection in Clinical Drug Development Xin Huang, AbbVie ; Paul Trow, AbbVie ; Yan Sun, AbbVie ; Viswanath Devanarayan, AbbVie
4:50 PM Big Data for Medical Research: A Unified Approach for Individualized Treatment Recommendation and Subgroup Identification Based on Electronic Medical Record Data Haoda Fu, Eli Lilly and Company ; Jin Zhou, University of Arizona
5:05 PM Development of Genetic Biomarkers in Drug Discovery and Early Drug Development Experiments Nolen Joy Perualila, Hasselt University ; Ziv Shkedy, Hasselt University ; Adetayo Kasim, Durham University
5:20 PM Biomarker-Based Dose-Finding Designs for Single- or Multiple-Agent Phase I Trials Yuan Xue, University of Virginia ; Mark Conaway, University of Virginia ; Feifang Hu, George Washington University
5:35 PM Center-Within-Trial Versus Trial-Level Evaluation of Surrogate Endpoints — Lindsay Renfro, Mayo Clinic ; Yuan Xue, University of Virginia ; Daniel Sargent, Mayo Clinic ; Qian Shi, Mayo Clinic



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