JSM 2011 Online Program
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Activity Details
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627 * | Thu, 8/4/2011, 8:30 AM - 10:20 AM | CC-D241 | |
Special Topics in Biopharmaceutical Statistics 1 — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): Anna Nevius, U.S. Food and Drug Administration/CVM | |||
8:35 AM | Statistical Evaluation of an In Vitro Screening Assay to Assess Cardiac Liabilities of Emerging Drugs — Lei Shu, Abbott Laboratories ; Gary Gintant, Abbott Laboratories ; Thomas C. Lin, Abbott Laboratories | ||
8:50 AM | Interval Estimation for Dichotomized Variables Derived from Continuous Measures in Establishing Acceptance Criteria for Biological Products — Jeongsook "Jessica" Kim, U.S. Food and Drug Administration ; Kyunghee Kim Song, U.S. Food and Drug Administration/CDRH | ||
9:05 AM | Preference-Based Approach to Estimating Treatment Acceptability and Effect in Compliant Patients in a Randomized Controlled Trial — Afisi Ismaila, McMaster University ; Stephen Walter, McMaster University | ||
9:20 AM | Copula-Based Likelihood Modeling and Estimation of Repeated-Measure Ordinal Data — Raghavendra Rao Kurada, Old Dominion University ; N. Rao Chaganty, Old Dominion University | ||
9:35 AM | A Comparison of Methods for the Analysis of Continuous Data from Sequential Parallel Comparison Design Trials — Allison Meisner, Boston University ; Michael Pencina, Boston University | ||
9:50 AM | Impact of Treatment Crossover on Survival Analysis in Clinical Trials — Yan Xu, University of California at Santa Barbara ; Ying Wan, Johnson & Johnson Pharmaceutical R&D, LLC | ||
10:05 AM | Floor Discussion |
2011 JSM Online Program Home
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