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45 | Sun, 8/9/2015, 2:00 PM - 3:50 PM | CC-618 | |
Topics in Clinical Trials 1 — Contributed Papers | |||
Biopharmaceutical Section , Biometrics Section | |||
Chair(s): Lisa Chen, Amgen | |||
2:05 PM | Missing Data Analysis in Crossover Studies with Baseline Measurements and Small Sample Sizes — Zifang Guo, Merck ; Yue Liu, Merck ; Devan Mehrotra, Merck | ||
2:20 PM | Bayesian Adaptive Designs in the Presence of Multiple Factors: Hyperbaric Oxygen Brain Injury Treatment (HOBIT) Phase II Trial — Byron J. Gajewski, University of Kansas Medical Center ; Scott M. Berry, Berry Consultants ; Gaylan L. Rockswold, Hennepin County Medical Center | ||
2:35 PM | A Bayesian Adaptive Design for Phase 2b Dose-Finding Using a Composite Endpoint — Norman Bohidar ; Kyle Wathen, Johnson & Johnson | ||
2:50 PM | Dose-Finding Methods Based on Cure Model Approach in Phase I Cancer Clinical Trials — Menghui Chen, Merck ; Yong Lin, Rutgers University ; Weichung Joe Shih, Rutgers University | ||
3:05 PM | Challenges on Pediatrics Clinical Trials — Annpey Pong | ||
3:20 PM | Improve the Prediction of Landmark Event Time by Incorporating Actual Enrollment Data — Yong Zhang, Novartis Pharmaceuticals ; Zhichao Sun, University of Michigan ; Kalyanee Appanna, Novartis Pharmaceuticals ; Cheng Zheng, Novartis Pharmaceuticals ; Kaushal Mishra, Novartis Pharmaceuticals ; Feng Tai, Novartis Pharmaceuticals ; Can Cai, Novartis Oncology | ||
3:35 PM | Missing Data Issue for Sedative Products in Human Abuse Potential Studies — Ling Chen, FDA |
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