JSM Preliminary Online Program
This is the preliminary program for the 2006 Joint Statistical Meetings in Seattle, Washington.

The views expressed here are those of the individual authors
and not necessarily those of the ASA or its board, officers, or staff.


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Legend: = Applied Session, = Theme Session, = Presenter, Sheraton Seattle Hotel & Towers = “S”
Washington State Convention & Trade Center = “CC”, Grand Hyatt Seattle = “H”

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161 Mon, 8/7/06, 12:30 PM - 1:50 PM CC-4C-2
Biopharmaceutical Section Roundtables with Lunch (fee event) - Roundtable Lnch
Biopharmaceutical Section
Organizer(s): Amit Bhattacharyya, GlaxoSmithKIine
ML09: New Development and Challenges in Phase I and Phase I/II Dose-Finding StudiesWeili He, Merck & Co., Inc.
ML10: Analysis and Evaluation of Safety Information from Clinical Trial DataH. Amy Xia, Amgen Inc.
ML11: Time-to-Event Analysis with Uncertain EndpointsLi Chen, Amgen Inc.
ML12: Analyses of Stratified Trials: Tips for Improving PowerDevan V. Mehrotra, Merck Research Laboratories
ML13: CANCELLED - Using Computer Simulation To Aid in Dose Selection in Clinical TrialsKenneth Liu, Merck & Co., Inc.
ML14: Assessing the Concordance of Two-Measurement MethodsJason Liao, Merck Research Laboratories
ML15: CANCELLED - Pharmacogenomics for Drug Development and Personalized MedicineXuejun Peng, Takeda Global Research and Development Center
ML16: CANCELLED - What To Do with Interaction Effects at Interim Analysis?Yuko Palesch, Medical University of South Carolina
ML17: Preparation of Interim Reports for Independent Data Monitoring Committee ReviewKyungMann Kim, University of Wisconsin-Madison
ML18: Statistical Design and Analysis Issues Associated with the Establishment of the Safety and Effectiveness of Medical DevicesGary Kamer, U.S. Food and Drug Administration
ML19: Issues in Planning Two-Arm Clinical Trials of Active DrugsSheela Talwalker, T'Walker Consulting
ML20: Analysis of Multiple Failure OutcomesGuowen Sun, sanofi-aventis
ML21: What Are the Statistical Issues in Subgroup Analysis - Design, Analysis, and Interpretation?Chul H. Ahn, U.S. Food and Drug Administration
ML22: Conducting Multiple Event Analysis in Clinical TrialsXiang Zhang, Amgen Inc.
 

JSM 2006 For information, contact jsm@amstat.org or phone (888) 231-3473. If you have questions about the Continuing Education program, please contact the Education Department.
Revised April, 2006