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RL16 Statistical Prediction in Adaptive Designs
*Ming-Dauh Wang, Eli Lilly and Company Keywords: Adaptive designs have been quickly adopted in recent years by pharmaceutical companies to enhance drug development efficiency, especially in pre-confirmatory clinical trials. Even though interim adaptation allows opportunities to adjust imperfect assumptions made prior to initiation of trials, it is also critical to consider inherent variability in future data to be collected when making interim decisions on trial design adjustment. Bayesian prediction is proposed for such a consideration. We will illustrate the approach with applications to interim data monitoring, sample size re-estimation, and adaptive patient allocation.
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Key Dates
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November 1, 2012
Online submission opens for session, short course, roundtable luncheon discussion, and Town Hall proposals -
December 31, 2012
Online submission for a session, short course, and Town Hall proposals closes @ 11:59 pm EDT -
February 12, 2013
Organizing/Planning Meeting, Shady Grove, MD -
March 1, 2013
Roundtable submission closes @ 11:59 pm EDT -
April 30 - May 22, 2013
Invited Abstract Submission Open -
June 4, 2013
Online Registration Opens -
August 9 - August 23, 2013
Invited Abstract Editing -
August 23, 2013
Short Course materials due from Instructors -
August 26, 2013
Housing Deadline -
September 9, 2013
Cancellation Deadline and Registration Closes @ 11:59 pm EDT -
September 16 - September 18, 2013
Marriott Wardman Park, Washington, DC









