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412 * ! | Tue, 8/11/2015, 2:00 PM - 3:50 PM | CC-610 | |
Practical Issues with the PFS Endpoint in Cancer Clinical Trial — Topic Contributed Papers | |||
Biopharmaceutical Section | |||
Organizer(s): Sudhakar Rao, Janssen R&D | |||
Chair(s): Sudhakar Rao, Janssen R&D | |||
2:05 PM | A Model to Analyze Survival in a Clinical Trial Where the Treatment Is Primarily Expected to Delay Disease Progression — Dianne M. Finkelstein, Massachusetts General Hospital/Harvard University ; David A. Schoenfeld, Massachusetts General Hospital/Harvard University | ||
2:25 PM | Is the Median PFS Difference Meaningful for Assessing Treatment Effect? — Steven Snapinn, Amgen | ||
2:45 PM | An Audit Plan in Oncology Clinical Trials — Steven Sun, Johnson & Johnson | ||
3:05 PM | Use of PFS and PFS2 in Cancer Clinical Trials — Tommy Fu, Celgene ; Marie-Laure Bravo, Celgene ; Chengqing Wu, Celgene ; Guang Chen, Celgene ; Zhinuan Yu, Celgene ; Qiang Xu, Celgene | ||
3:25 PM | Discussant: Surya Mohanty, Johnson & Johnson | ||
3:45 PM | Floor Discussion |
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