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471 * Wed, 8/1/2012, 8:30 AM - 10:20 AM CC-Room 23B
Innovations in Design and Analysis of Clinical Trials — Contributed Papers
Biopharmaceutical Section
Chair(s): Chava Zibman, FDA
8:35 AM Random Forest with Regression in the Nodes Georgiy Bobashev, RTI International ; Barry Eggleston, RTI International ; Nikhil Garge, RTI International
8:50 AM Parametric Models for MRI Count Data in Multiple Sclerosis Clinical Trials: A Robustness Study Mallikarjuna Rettiganti, University of Arkansas for Medical Sciences ; Haikady Nagaraja, The Ohio State University
9:05 AM Analytical Methodologies for Clinical Endpoint Data with Excessive Zero Nancy Liu, Merck ; Amarjot Kaur, Merck Research Laboratories ; Jing Li, Merck ; Ziliang Li, Merck
9:20 AM Oracle, Robust, and Best Linear Model Average Estimation in Randomized Trial Kwun Chuen Chan, University of Washington
9:35 AM Global Summary of Treatment Impact Using Multiple Patient Outcomes Brian Claggett, Harvard University ; Lu Tian, Stanford University ; Sihai Dave Zhao, Harvard School of Public Health ; Lee-Jen Wei, Harvard University
9:50 AM Power Analysis for Testing Treatment Effect with a Covariate and a Covariate-Dependent Stratification Factor Chii-Dean Lin, San Diego State University ; Tao Lin, Allergon ; Chien-Feng Chen, Otsuka Pharmaceutical ; Larry Shen, Amylin Pharmaceutical
10:05 AM A Hybrid Bootstrap Approach to Interim Analyses of Time-to-Event Data Using Kaplan-Meier Methods Kevin Lawson, PPD ; Aaron C Camp, PPD ; Austin L Hand, PPD



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