2006 Presentations

Session	Speaker	Presentation
M1	Stephan Ogenstad	Simulation for Designing and Analyzing Clinical Trials
M-2	Dejun Tang	Comparison of Statistical Analysis Methods using Modeling and Simulation in Modern Protocol Design
M-3	Naitee Ting	Dose Finding in Drug Development: Study Design Considerations
M-4	Mark J. van der Laan	Resampling Based Multiple Testing: Controlling Proportion of False Positives
M-5	Michael O'Connell	Standardized Graphics for Safety using S-Plus Software
M-6	Ralph Raymond & Frank Shen	Model Based Adaptive Design
M-7	Tim Montague	Bioequivalence Trials Designed Using Adaptive Methodologies
Keynote Address	Greg Campbell	The World of Medical Devices and its Increasing Impact on Pharmaceutical Statistics
T-1	Rong Liu	A Comparison of Methods for Longitudinal Data Missing Due to Truncation
T-2	Julia Wang & Akiko Okamoto	Rescue Behavior and Imputation Strategies in Analgesic Studies
T-3	Robert E. Johnson	Multivariate Assays with Values Below the Lower Limit of Quantitation: Parametric Estimation by Imputation and Maximum Likelihood
T-4	Andrew Strahs	Variability in Gene Expression in Healthy Volunteers
T-5	Shein-Chung Chow & Mark Chang	Adaptive Design Methods in Clinical Trials-Part 1 Adaptive Design Methods in Clinical Trials-Part II
W-FDA	Mohammad Huque	On Some Statistical Considerations in Planning and Testing of Multiple Endpoint Hypotheses in Clinical Trials
W-FDA	Guoxing (Greg) Soon	Issues and Considerations for Composite Endpoints Use in Clinical Trials
W-FDA	Atiar Rahman	Recent Results concerning Multiplicities in Animal Carcinogenicity Studies
W-FDA	Alex Dmitrienko	Tree-structured Gatekeeping Procedures in Clinical Trials with Multiple Objectives

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2006 Presentations