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

For information, contact or phone (888) 231-3473.

If you have questions about the Continuing Education program, please contact the Education Department.