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546 | Wed, 8/12/2015, 10:30 AM - 12:20 PM | CC-616 | |
Adaptive Design III — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): LingLing Han, | |||
10:35 AM | Interim Equivalence Test with Application in Drug Development — Yansong Cheng | ||
10:50 AM | Issues in Planning and Conduct of Sample Size Re-Assessment in Medical Device Trials — Laura Lu, FDA/CDRH | ||
11:05 AM | An ROC-Based Approach to Interim Go/No-Go Decision-Making and Design Optimization in Late Phase Clinical Trials — Deli Wang, AbbVie ; Cui Lu, AbbVie ; Lanju Zhang, AbbVie ; Bo Yang, AbbVie Pharmaceutical Research & Development | ||
11:20 AM | Recurrent Event Analyses Illustrated in the Pivotal Exacerbation Study SPARK in the Respiratory Area — Hua Li, Novartis ; Paul Gallo, Novartis Pharmaceuticals ; Richard Cook, University of Waterloo | ||
11:35 AM | Robust Optimal Interval Design with an Application to Dose-Finding in Drug-Combination Trials — Ruitao Lin, The University of Hong Kong ; Guosheng Yin, The University of Hong Kong | ||
11:50 AM | Multiple Comparisons with Two Controls for Ordered Categorical Responses — Ping Yang, The Chinese University of Hong Kong ; Siu Hung Cheung, The Chinese University of Hong Kong ; Wai Yin Poon, The Chinese University of Hong Kong | ||
12:05 PM | Floor Discussion |
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