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Activity Details


31 * Sun, 8/3/2014, 2:00 PM - 3:50 PM CC-258C
Power and Sample Size — Contributed Papers
Biopharmaceutical Section
Chair(s): Stephen Lane, GlaxoSmithKline   
2:05 PM Simulations on Sample Sizes and Powers Calculations for a Registry Vaccine Study John Liang, Pfizer ; Scott Patterson, Pfizer
2:20 PM Experimental Design and Sample Size for Long-Term Carcinogenicity Studies: Statistical Considerations Lei Shu, AbbVie ; Lanju Zhang, AbbVie ; Sherry Morgan, AbbVie
2:35 PM Random-Effects Linear Modeling and Sample Size Computations for Two Special Crossover Designs of Average Bioequivalence Studies Francisco J. Diaz, University of Kansas Medical Center ; Michel Berg, University of Rochester Medical Center ; Ron Krebill, University of Kansas Medical Center ; Timothy Welty, Drake University ; Barry E. Gidal, University of Wisconsin ; Rita Alloway, University of Cincinnati ; Michael Privitera, University of Cincinnati Neuroscience Institute
2:50 PM Power Analyses Based on Negative Binomial Models for Two Period Cross-Over Trials Involving Overdispersed Count Data Mallik Rettiganti, University of Arkansas for Medical Sciences ; Haikady Nagaraja, Ohio State University
3:05 PM Use of a Posterior Beta Distribution with Recurrent Event Data Jerry Weaver, Novartis
3:35 PM Statistical Endpoint Selection for Recurrent Events in Clinical Trials Xiaohai Wan ; Qianying Liu, University of Chicago ; Nathalie Ezzet, Novartis ; Paul Gallo, Novartis



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