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This is the preliminary program for the 2008 Joint Statistical
Meetings in Denver, Colorado.
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The views expressed here are those of the individual authors and not necessarily those of the ASA or its board, officers, or staff. Back to main JSM 2008 Program page |
= Applied Session,
= Theme Session,
= Presenter|
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240
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Tue, 8/5/08, 8:30 AM - 10:20 AM | CC-601 |
| Statistical Issues in Oncology Trials - Contributed - Papers | ||
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Biopharmaceutical Section, Biometrics Section |
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| Chair(s): Yonggang Zhao, Wyeth Research | ||
| 8:35 AM |
Family of Optimum M-Stage Designs for Single Arm Phase II Oncology Clinical Trials — Muhammad Jalaluddin, Novartis Pharmaceuticals
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| 8:50 AM |
Relationship Between Type I/II Errors and Frequency of Progression Assessment — Xiaoping Jiang, U.S. Food and Drug Administration; Kun He, U.S. Food and Drug Administration; Rajeshwari Sridhara, U.S. Food and Drug Administration
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| 9:05 AM |
Consequences of Asymmetry in Progression Assessments — Shenghui Tang, U.S. Food and Drug Administration; Chris Holland, U.S. Food and Drug Administration; Rajeshwari Sridhara, U.S. Food and Drug Administration
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| 9:20 AM |
Evaluation of Time-to-Progression: Where Your Censor Matters? — Chia-wen Ko, U.S. Food and Drug Administration; Somesh Chattopadhyay, U.S. Food and Drug Administration; Rajeshwari Sridhara, U.S. Food and Drug Administration
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| 9:35 AM |
Decision Rules in Phase II and III Oncology Studies — Pralay Mukhopadhyay, Bristol-Myers Squibb Company; Thomas Kelleher, Bristol-Myers Squibb Company
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| 9:50 AM |
Dose Reduction Profiles for Combination Drug Studies — John J. Peterson, GlaxoSmithKline Pharmaceuticals
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| 10:05 AM |
Sensitivity Analysis for Treatment Drop-In in Oncology Clinical Trials — Cheng A. Rong, Amgen, Inc; Michael Wolf, Amgen, Inc; Zhiying J. Pan, Amgen, Inc; Xiang C. Zhang, Amgen, Inc
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JSM 2008
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. |