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This is the preliminary program for the 2006 Joint Statistical
Meetings in Seattle, Washington.
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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 2006 Program page |
= Applied Session,
= Theme Session,
= Presenter, Sheraton Seattle Hotel & Towers = “S”
154
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Mon, 8/7/06, 10:30 AM - 12:20 PM | CC-2A |
| Adaptive Methods - Contributed - Papers | ||
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Biopharmaceutical Section |
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| Chair(s): Wei Zhong, ICON Clinical Research | ||
| 10:35 AM |
A Two-Stage Adaptive Design for Phase III Trials To Establish Noninferiority and Superiority — Yulan Li, Novartis Pharmaceuticals Corporation; Qing Liu, Johnson & Johnson; Jeffrey Maca, Novartis Pharmaceuticals Corporation
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| 10:50 AM |
Confidence Intervals Following an Adaptive Group Sequential Design — Cyrus Mehta, Cytel Inc.
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| 11:05 AM |
Implementing Adaptive Designs in Clinical Trials: Risks and Benefits — Christopher Khedouri, U.S. Food and Drug Administration; Thamban Valappil, U.S. Food and Drug Administration; Mohammad Huque, U.S. Food and Drug Administration
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| 11:20 AM |
Dynamic Treatment Allocation and Randomization Tests in Clinical Trials — Lee-Lian Kim, Centocor R&D, Inc.; Yaung-Kaung Shen, Centocor R&D, Inc.; Jewel Johanns, Centocor R&D, Inc.; Aparna Raychaudhuri, Centocor R&D, Inc.
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| 11:35 AM |
Resampling Methods for Adaptive Designs — Hui Zhang, Bristol-Myers Squibb Company
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| 11:50 AM |
Evaluating Exploratory and Confirmatory Evidience Collectively — Qian Li, U.S. Food and Drug Administration
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| 12:05 PM |
Adjusted Two-Sided Combination Tests for Adaptive Clinical Trials — Zhilong Yuan, Johnson & Johnson Pharmaceutical R&D; Yang Song, Johnson & Johnson Pharmaceutical R&D; Xiaolong Luo, Johnson & Johnson Pharmaceutical R&D; George Chi, Johnson & Johnson Pharmaceutical R&D
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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. |