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This is the preliminary program for the 2007 Joint Statistical
Meetings in Salt Lake City, Utah.
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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 2007 Program page |
= Applied Session,
= Theme Session,
= Presenter
273
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Tue, 7/31/07, 10:30 AM - 12:20 PM | CC-355 D |
| Adaptive Medical Device Clinical Trials - Topic Contributed - Papers | ||
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Biopharmaceutical Section, ENAR |
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| Organizer(s): Lilly Yue, Food and Drug Administration | ||
| Chair(s): Laura Thompson, Food and Drug Administration | ||
| 10:35 AM |
Comparison of Two Adaptive Randomization Methods in Multicenter Clinical Trials —  Lei Peng, Abbott Vascular
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| 10:55 AM |
Data Analysis in a Medical Device Trial When Planned Randomized Enrollment Is Too Slow — Yonghong Gao, Food and Drug Administration; Gerry Gray, Food and Drug Administration
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| 11:15 AM |
Statistical Analysis for Two-Stage Adaptive Design with Different Study Endpoints — Shein-Chung Chow, Duke University; Siu-Keung Tse, Hong Kong City University
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| 11:35 AM |
One Adaptive Design and Its Application to Medical Device PMA Study — Xiaolong Luo, Johnson & Johnson PRD; David Snead, Cordis, a Johnson & Johnson Company; Dennis Donohoe, Cordis, a Johnson & Johnson Company
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| 11:55 AM |
Flexible Designs in Clinical Trials: Case studies — Ning Li, Food and Drug Administration
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| 12:15 PM | Floor Discussion | |
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JSM 2007
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. |