Keyword Search
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CC = Baltimore Convention Center, H = Hilton Baltimore
* = applied session ! = JSM meeting theme
Keyword Search Criteria: Study Design returned 17 record(s)
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Sunday, 07/30/2017
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Techniques for Matched Randomization in Sequential Enrollment Trials
Jonathan J Chipman, Vanderbilt University; Cole Beck, Vanderbilt University; Robert A Greevy, Jr, Vanderbilt University
2:05 PM
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A Maximum Likelihood Approach to Power Calculations for Stepped Wedge Designs of Binary Outcomes
Xiaomei Liao, AbbVie; Lauren Kunz, NIH; Sharon-Lise Normand, Harvard Medical School; Donna Spiegelman, Harvard T.H. Chan School of Public Health
4:05 PM
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A Cautionary Note on the Validation Method for Molecular Classification Studies
Li-Xuan Qin, Memorial Sloan Kettering Cancer Center
4:55 PM
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Monday, 07/31/2017
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Essential Role of Statistics in Publishing Medical Research Papers
Daniel Byrne, Vanderbilt University; Henry J Domenico, Vanderbilt; Li Wang, Vanderbilt
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dECiDe: software developed by Cytel and AstraZeneca for early clinical study design
Patrick D. Mitchell, Early Clinical Development AstraZeneca; Dominic Magirr, AZ IMED Biotech Unit, ECD Biometrics; Elizabeth Pilling, AZ IMED Biotech Unit, ECD Biometrics; James Matcham, AZ IMED Biotech Unit, ECD Biometrics; Jaydeep Bhattacharyya, Cytel Inc.; Charles Liu, Cytel Inc.
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Wednesday, 08/02/2017
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Designing a Robust Monitoring Scheme for Natural Resources at a Continental Scale
Emily L Weiser, U.S. Geological Survey; James E. Diffendorfer, U.S. Geological Survey; Laura López-Hoffman, The University of Arizona; Darius J Semmens, U.S. Geological Survey; Wayne E Thogmartin, U.S. Geological Survey
8:55 AM
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Introductory Statistics Students' Conceptual Understanding of Study Design and Conclusions
Elizabeth Fry, University of Minnesota
9:35 AM
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Inferences from Various Study Designs for Companion Diagnostic Device Evaluation
Jeng Mah, Beckman Coulter
9:50 AM
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Biomarker Based Study Design with Multiple Single Arms
Shiling Ruan, Novartis
11:35 AM
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Current Practices in Reporting Trial Simulations for Adaptive Study Designs
cristiana mayer, Janssen R&D; Parvin Fardipour, ICON
2:05 PM
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Proposed Guidelines for Interim Monitoring of Prospective Observational Studies Planning to Invoke Propensity-Scoring as the Primary Analysis
Michael Swartz, The University of Texas Health Science Center At Houston, School of Public Health; Thomas Jay Greene, The University of Texas Health Science Center at Houston, School of Public Health; Erin E Fox, The University of Texas Health Science Center, Center for Translational Injury Research; Savitri N. Appana, The University of Texas Health Science Center at Houston; Misung Yi, The University of Texas Health Science Center at Houston, School of Public Health; Soeun Kim, The University of Texas Health Science Center at Houston, School of Public Health; Elysia A. Garcia, The University of Texas Health Science Center at Houston, School of Public Health; Jada M. Johnson, The University of Texas Health Science Center at Houston, School of Public Health; Jeanette Podbielski, The University of Texas Health Science Center, Center for Translational Injury Research; Jeffrey S. Tomasek, The University of Texas Health Science Center, Center for Translational Injury Research; Charles E. Wade, The University of Texas Health Science Center, Center for Translational Injury Research; John B. Holcomb, The University of Texas Health Science Center at Houston; Stacia M DeSantis, UTHealth SPH
2:05 PM
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On Sensitivity Value of Pair-Matched Observational Studies
Qingyuan Zhao, University of Pennsylvania
2:20 PM
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Immunogenicity Study Design for Biosimilar Approval
Junshan Qiu, FDA; Mike Mikailov, FDA; Ram Tiwari, FDA/CDER/OT/OB
3:35 PM
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