TL01: Logistics and Implementation of Adaptive Trial Design
*Eva R Miller, ICON Clinical Research Keywords: Participants at this roundtable will discuss real world experiences in the implementation of adaptive trials. Statisticians who have actually conducted adaptive trials are welcome. Statisticians who are about to conduct adaptive trials are welcome to learn from the "veterans". Topics include: roles and responsibilities of an unblinded statistician, data lag, working with several data sources, and managing communications of unblinded information, randomization and drug supply. If a discussion leader from the FDA were interested in joining. he/she would be most welcome.
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Key Dates
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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