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Legend: Palais des congrès de Montréal = CC, Le Westin Montréal = W, Intercontinental Montréal = I
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Activity Details

31 Sun, 8/4/2013, 2:00 PM - 3:50 PM CC-512g
Methodology for Early-Stage Oncology Trials — Contributed Papers
Biopharmaceutical Section , Biometrics Section , Korean International Statistical Society
Chair(s): Chunyan Cai, UT Health Science Center at Houston
2:05 PM Evaluating Probability of Success in Oncology Drug Development Di Li, Eisai Inc
2:20 PM Bivariate Continual Reassessment Method (BCRM) Applied to Oncology Dose Escalation Study Yinghua (Grace) Zhang, GSK ; Jie Ding, GSK
2:35 PM An 'Early-Go' Design for Single-Arm, Two-Stage, Phase II Clinical Trials William E. Brady, Roswell Park Cancer Institute ; Gregory Wilding, Roswell Park Cancer Institute
2:50 PM Probability-Guided 3+3 Design in Phase I Dose-Escalation Study Yung-Seop Lee, Dongguk Univ. ; Jung Wook Park, Astellas Pharma Global Development, Inc.
3:05 PM Enrollment and Stopping Rules for Managing Toxicity in Phase II Oncology Trials with Delayed Outcome Guochen Song, Quintiles ; Anastasia Ivanova, Department of Biostatistics, UNC Chapel Hill
3:20 PM Using the Facts Recommender in Oncology Dose Escalation Trials: A Comparison of Dose Escalation Decisions Suggested by the Recommender with Actual Decisions Made by Project Teams Sharon Murray, GlaxoSmithKline ; Tom Parke, Tessella plc ; Allison Florance, GlaxoSmithKline ; Alun Bedding, GlaxoSmithKline
3:35 PM Alternative Designs for Phase II Clinical Trials When Attained Sample Sizes Are Different from Planned Sample Sizes Myron Chang, University of Florida

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