JSM 2015 Preliminary Program

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Legend: Washington State Convention Center = CC, Sheraton Seattle = S, Grand Hyatt = GH and The Conference Center = TCC
* = applied session       ! = JSM meeting theme

Activity Details


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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