This is the program for the 2010 Joint Statistical Meetings in Vancouver, British Columbia.

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Keyword Search Criteria: utility returned 16 record(s)
Monday, 08/02/2010
Simulation of Kidney Paired Donation Programs
Yijiang (John) Li, University of Michigan; Yan Zhou, University of Michigan; John David Kalbfleisch, University of Michigan; Peter Song, University of Michigan


Statistical Reasons Why Preference-Scored Measures of HRQoL Disagree
Mari Palta, University of Wisconsin


Futility Assessment Utilizing Conditional Power in a Phase III Clinical Trial
Yan Sun, Amgen Inc.
8:35 AM

Sample Size and Power Considerations for Futility Trial Design: Buying Power vs. Spending Beta
Thomas Dobbins, Merck & Co., Inc.
8:50 AM

Bayesian Decision Analysis for Diagnostic Procedures
Ying Lu, Stanford University; John Kornak, University of California, San Francisco
9:35 AM

Should the Conditional Type I Error Be Controlled?
Tie-Hua Ng, FDA
9:50 AM

Two-Stage Designs with Additional Futility Tests for Phase II Clinical Trials with Heterogeneous Patient Populations
Myron N. Chang, University of Florida; Sin-Ho Jung, Duke University
10:05 AM

Tuesday, 08/03/2010
Accuracy of Nonparametric Price Indexes Relative to a Parametric Price Index of an Estimated Cobb-Douglas Marginal Utility Model
Peter Zadrozny, Bureau of Labor Statistics
11:35 AM

Optimal Phase II Decision Rules in a Seamless PhaseII/III Clinical Trial
Bo Jin, Merck Research Laboratories
2:05 PM

Wednesday, 08/04/2010
Utility of Positive Controls in Assessing QT Interval Sensitivity
Alan Y. Chiang, Eli Lilly and Company
9:05 AM

An Adaptive Futility Monitoring Method with Time-Varying Conditional Power Boundary
Ying Zhang, The University of Iowa; William Clarke, The University of Iowa
10:55 AM

The Role of Bayesian Statistics in Confirmatory Drug Development Trials
David Ohlssen, Novartis Pharmaceuticals Corporation
2:30 PM

Adding a Prediction Interval Futility Analysis to a Group Sequential Trial
John Loewy, ARIAD Pharmaceuticals; David Dorer, ARIAD Pharmaceuticals
3:25 PM

Thursday, 08/05/2010
Risk Models for Deciding Whether to Take Tamoxifen to Prevent Breast Cancer and for Allocating Public Health Resources
Mitchell H. Gail, National Cancer Institute
8:35 AM

Design and Trial Operational Considerations for a Phase II Two-Stage Adaptive Trial
Weili He, Merck & Co., Inc.; Madhuja Mallick, Merck & Co., Inc.; Yevgen Tymofyeyev, Merck & Co., Inc.; James A. Bolognese, Cytel Inc.
10:55 AM

Analysis of Discrete Choice Models with Latent Variable in Unobserved Component of Utility
Woosuk Kim, University of Cincinnati; Seongho Song, University of Cincinnati; Young Seuk Cho, Pusan National University
11:05 AM




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