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549 | Wed, 8/12/2015, 10:30 AM - 12:20 PM | CC-617 | |
Power and Sample Size II — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): Grace Liu, Johnson & Johnson, Janssen R&D | |||
10:35 AM | Using Mixture Model for the Time-to-Event Data in Oncology Studies — Weichao Bao, Novartis Oncology ; Jason Liao, Novartis Pharmaceuticals | ||
10:50 AM | Testing the Difference in the Cumulative Risk Distributions of Two Events — Sujata Patil, Memorial Sloan Kettering Cancer Center ; Deborah Kuk, Memorial Sloan Kettering Cancer Center | ||
11:05 AM | A Population-Enrichment Adaptive Design Strategy for Vaccine Efficacy Trial — Shu-Chih Su, Merck Research Laboratories ; Ivan S.F. Chan, Merck Research Laboratories | ||
11:20 AM | Joint Analysis of Two Distinct but Interrelated Disease Processes in Multiple Sclerosis — Tristan Massie, FDA | ||
11:35 AM | Metrics for Comparison of Phase I Dose-Finding Designs — Hong Wang, University of Pittsburgh Cancer Institute | ||
11:50 AM | Statistical Approaches to Outliers Test in Bioassay Analytical Testing Data — Lingmin Zeng, MedImmune ; Binbing Yu, MedImmune ; Harry Yang, MedImmune | ||
12:05 PM | Multiplicity Adjustment for Noninferiority Design — Jing Zhao, Merck Research Laboratories |
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