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700 | Thu, 8/13/2015, 10:30 AM - 12:20 PM | CC-619 | |
Topics in Clinical Trials 3 — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): Grace Hyun Kim, UCLA | |||
10:35 AM | Adjust for Subsequent Therapies in Overall Survival Analyses — Lixia Pei, Johnson & Johnson, Janssen R&D ; Grace Liu, Johnson & Johnson, Janssen R&D ; Youn Park, Janssen | ||
10:50 AM | Bioequivalence Study Design with Unknown Variance on PK Parameters — Jialin Xu, Merck | ||
11:05 AM | Adaptive Monitoring of HIV Prevention Trials in the Presence of Extreme Treatment Effect — William Koh ; Scott Emerson, University of Washington | ||
11:20 AM | Improved Efficiency in Relative Risk Estimation and Hypothesis Testing with Small Samples — Rengyi Xu, University of Pennsylvania ; Pamela Shaw, University of Pennsylvania ; Devan Mehrotra, Merck | ||
11:35 AM | Software for Meta-Analysis in Clinical Studies — Qiaolin Chen, Novartis Pharmaceuticals ; Siyu Li, Novartis Pharmaceuticals | ||
11:50 AM | Patient-Specific Meta-Analysis with Application to a Genomic Prostate Cancer Diagnostic — Michael Crager, Genomic Health, Inc. ; Nan Zhang, Genomic Health, Inc. ; Tara Maddala, Genomic Health, Inc. |
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