This is the program for the 2010 Joint Statistical Meetings in Vancouver, British Columbia.
Activity Details
569 ! | Wed, 8/4/2010, 2:00 PM - 3:50 PM | CC-220 (West) |
Methods, Practical Experiences, and Strategies for Adaptive Design Clinical Trials — Topic Contributed Papers | ||
Biopharmaceutical Section , Section for Statistical Programmers and Analysts | ||
Organizer(s): Sue-Jane Wang, FDA | ||
Chair(s): Sue-Jane Wang, FDA | ||
2:05 PM | Sequential Design of Phase II--III Cancer Trials — Tze Leung Lai, Stanford University ; Philip Lavori, Stanford University ; Mei-Chiung Shih, Stanford University | |
2:25 PM | Adaptive Dose Finding Using the 'Maximizing Procedure': Case Study and Missing Data Simulation — Kenneth Liu, Merck & Co., Inc. | |
2:45 PM | Informed Decisionmaking Using Modeling and Simulation: Case Study of a Selective PDE5 Inhibitor for the Treatment of BPH — Patrick John Johnson, Vifor Pharma Ltd. | |
3:05 PM | Strategies for Setting Up the Logistics in Early Phase Adaptive Design Clinical Trials — Eva R. Miller, ICON Clinical Research | |
3:25 PM | Adding a Prediction Interval Futility Analysis to a Group Sequential Trial — John Loewy, ARIAD Pharmaceuticals ; David Dorer, ARIAD Pharmaceuticals | |
3:45 PM | Floor Discussion |
2010 JSM Online Program Home
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