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85 | Sun, 8/9/2015, 4:00 PM - 5:50 PM | CC-611 | |
Biomarkers and Endpoint Validation 1 — Contributed Papers | |||
Biopharmaceutical Section , Biometrics Section | |||
Chair(s): Samir Lababidi, | |||
4:05 PM | Sequential Monitoring of Clinical Trials with a Stepped Wedge Design — Siobhan Brown, University of Washington ; Abigail Shoben, The Ohio State University | ||
4:20 PM | Statistics to Aid Decision Making for Early-Phase Cancer Trials with Time-to-Event Endpoints — Shaoyi Li, Celgene | ||
4:35 PM | Sequential Basket Design with Subgroups Defined by Predictive Biomarker and Cancer — Shuai Yuan, Merck | ||
4:50 PM | Using Correlation Patterns of Study Findings to Assess Data Quality in Clinical Trials — Richard Zink, SAS Institute | ||
5:05 PM | MOST: Multi-Stage Optimal Sequential Trial Design for Phase II Clinical Trials with Biomarker Subgroups — Yong Zang, Florida Atlantic University | ||
5:20 PM | Model-Based Meta-Analysis of Clinical Dose Response for Biological Products — Joseph Wu, Pfizer Inc. ; Anindita Banerjee, Pfizer Inc. ; Bo Jin, Pfizer Inc. ; Sandeep Menon, Pfizer Inc. ; Steven Martin, Pfizer Inc. | ||
5:35 PM | Floor Discussion |
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