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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296 Tue, 8/8/06, 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
TL10: Contemporary Issues in Data Monitoring CommitteesDavid Kerr, Axio Research
TL11: Controlling Error Rate in Safety Assessments from a Regulatory PerspectiveQian Li, U.S. Food and Drug Administration
TL12: The Use of Targeted Designs in Clinical TrialsGerald Crans, Eli Lilly and Company; Matthew Rotelli, Eli Lilly and Company
TL13: CANCELLED - Statistical Concerns and Methodology Regarding Cognitive and Psychomotor Endpoints in Early Development (Phase I Trials)Cynthia Gargano, Merck & Co., Inc.
TL14: Preferred Methods of Dealing with Missing Data in Clinical TrialsRukmini Rajagopalan, Abbott Laboratories
TL15: Decision Rules Based on Multiple Endpoints in Clinical TrialsAlex Dmitrienko, Eli Lilly and Company
TL16: Patient-Reported Outcomes: Issues Related to the Collection and Analysis, Including Measurement Reliability and SensitivityTammy J. Massie, U.S. Food and Drug Administration
TL17: Statistician's Role in PK/PD Modeling and Clinical Trial SimulationHaiyuan Zhu, Merck Research Laboratories
TL18: Retrospective Testing for Baseline Variables Comparability and Subsequent Covariate Adjustments for Significant Imbalance: Good Clinical Practice or Bad Statistical Practice?Abdul Sankoh, sanofi-aventis
TL19: CANCELLED - Statistical Issues Regarding Experimental MedicineJames Bolognese, Merck Research Laboratories
TL20: Bayesian Dose-Finding Strategies for Phase I Oncology TrialsGlen Laird, Novartis Pharmaceuticals Corporation
TL21: On the Evaluation of Benefit and Risk: the Tools We Have and How They HelpYili Pritchett, Abbott Laboratories
TL22: Use of Adaptive Clinical Trial Designs in Clinical Development for Product RegistrationLaura Meyerson, Biogen Idec
 

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