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191 | Mon, 8/10/2015, 10:30 AM - 12:20 PM | CC-310 | |
Biomarkers and Endpoint Validation II — Contributed Papers | |||
Biopharmaceutical Section , Biometrics Section | |||
Chair(s): Feng Gao, Takeda Pharmaceuticals | |||
10:35 AM | A Proposed Study Design for QT Assessment Using Exposure-Response Modeling — Fang Liu, Merck ; Devan Mehrotra, Merck ; Deborah Panebianco, Merck ; Kuenhi Tsai, Merck | ||
10:50 AM | Comparison of Missing Data Imputation Methods and Statistical Analysis Methods by Simulation — Wenqing Li ; Yun Chon, Amgen ; Yi Wang, Amgen | ||
11:05 AM | Early Stopping for Futility or Efficacy in Group-Sequential Clinical Trials with Multiple Co-Primary Endpoints — Koko Asakura, National Cerebral and Cardiovascular Center ; Toshimitsu Hamasaki, National Cerebral and Cardiovascular Center ; Scott R. Evans, Harvard University | ||
11:20 AM | Design and Analysis of Clinical Trials with Biologics Using Dose Time Response Models — Markus Reiner Lange, Novartis Pharma AG ; Heinz Schmidli, Novartis Pharma AG | ||
11:35 AM | Using Software to Search for Optimal Cross-Over Designs — Byron Jones, Novartis Pharma AG | ||
11:50 AM | The Effect of Measurement Error on Biomarker Adaptive Threshold Design — Hong Tian, Janssen Research and Development ; Kevin Liu, Janssen R&D | ||
12:05 PM | Estimating Adverse Event Rate Differences Using Data from Blinded Trials: The Canary in the Coal Mine — A. Lawrence Gould, Merck Research Laboratories ; William W.B. Wang, Merck Research Laboratories |
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