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Activity Details


319 * Tue, 8/5/2014, 10:30 AM - 12:20 PM CC-156A
Impact of Missing Data on Trial Success and Approval of Potentially Efficacious Therapies — Topic Contributed Papers
Biopharmaceutical Section
Organizer(s): Abdul J. Sankoh, Vertex Pharmaceuticals
Chair(s): Yanqiong Zhang, Vertex Pharmaceuticals   
10:35 AM Mitigating Missing Data: A Proactive Approach for Minimizing Occurrence in Clinical Trials Carol Robertson-Plouch, Eli Lilly and Company ; Sarah Witt, Eli Lilly and Company ; Tina Oakes, Eli Lilly and Company
10:55 AM Considerations for Prevention and Handling of Missing Data in Clinical Trials — Cynthia DeSouza, Vertex Pharmaceuticals ; Abdul J. Sankoh, Vertex Pharmaceuticals
11:15 AM A Taxonomy of Estimands for Regulatory Clinical Trials with Discontinuations Thomas Permutt, FDA
11:35 AM Missing Data in Clinical Trials:Tryng to Select Reasonable Approaches and Sorting Out Their Effect on Analysis Ralph D'Agostino Sr., Boston University
11:55 AM Discussant: Boguang Zhen, CBER/FDA
12:15 PM Floor Discussion



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