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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
145
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Mon, 7/30/07, 10:30 AM - 12:20 PM | CC-155 F |
| Statistical Issues in Noninferiority and Equivalence Trials - Contributed - Papers | ||
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Biopharmaceutical Section, Biometrics Section |
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| Chair(s): Stephanie Dunbar, Merck & Co., Inc. | ||
| 10:35 AM |
Generalized Mixed Models for Noninferiority Trials — Robert Abugov, Food and Drug Administration
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| 10:50 AM |
Trials and Tribulations in Choosing Noninferiority Margins — John Johnson, Cato Research, Ltd.
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| 11:05 AM |
A Testing Strategy for Noninferiority and/or Superiority Hypotheses on Multiple Endpoints — Xiaohui Luo, Merck & Co., Inc.; Jianjun Li, Merck & Co., Inc.
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| 11:20 AM |
New Tests for Assessing Noninferiority and Equivalence from Survival Data — Kallappa Koti, Food and Drug Administration
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| 11:35 AM |
A Multivariate Test for Population Bioequivalence — Inna Chervoneva, Thomas Jefferson University; Terry Hyslop, Thomas Jefferson University; Walter W. Hauck, Kimmel Cancer Center at Jefferson
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| 11:50 AM |
Estimation of Long-Term Vaccine Efficacy and Waning Effects Using Surveillance Interval Data — Martha Lee, Food and Drug Administration; Tsai-Lien Lin, Food and Drug Administration
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| 12:05 PM |
An Equivalence Test Based on the Duration of Treatment Effect as Measured by Median Time-to-Event — Suriani Pokta, Allergan, Inc.; Jihao Zhou, Allergan, Inc.
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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. |