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701 | Thu, 8/13/2015, 10:30 AM - 12:20 PM | CC-618 | |
Dose Finding, Dose Response in Clinical Trials — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): Bojena Bitman, Amgen | |||
10:35 AM | Dose-Response Modeling Methods to Identify the Minimum Effective Dose (MED) — Danielle Sullivan ; Yihan Li, AbbVie ; Wangang Xie, AbbVie ; Su Chen, AbbVie ; Yuanyuan Tang, AbbVie ; Ying Zhang, AbbVie ; Yijie Zhou, AbbVie | ||
10:50 AM | A Bayesian Repeated Measures Design with Temporal Trend for Delayed Toxicity Outcomes — Rui Qin, Mayo Clinic ; Jun Yin, Mayo Clinic ; Sumithra J. Mandrekar, Mayo Clinic ; Daniel Sargent, Mayo Clinic | ||
11:05 AM | Centered Isotonic Regression: Point and Interval Estimation for Dose-Response Studies — Assaf Oron, Seattle Children's Research Institute ; Nancy Flournoy, University of Missouri - Columbia | ||
11:20 AM | A Response-Adaptive Covariate-Balanced Randomization for Multi-Arm Clinical Trials — Cassandra Ballou, OHSU ; Yiyi Chen, Oregon Health & Science University | ||
11:35 AM | Bayesian Dose-Finding Designs for Drug Combination Using the Times to Response-Toxicity Trade-Offs Assuming Partial Ordering — Xiao Su, The University of Texas Health Science Center ; Yisheng Li, MD Anderson Cancer Center | ||
11:50 AM | A New Bayesian Dose-Finding Design for Drug Combination Trials — Jin Xu, East China Normal University ; Rongji Mu, East China Normal University | ||
12:05 PM | Selection of Multiplicity Adjustment Strategy in Confirmatory Trials with a Targeted Subgroup — Cheng Zheng, Novartis Pharmaceuticals ; Zhichao Sun, University of Michigan ; Kalyanee Appanna, Novartis Pharmaceuticals ; Kaushal Mishra, Novartis Pharmaceuticals ; Yong Zhang, Novartis Pharmaceuticals ; Feng Tai, Novartis Pharmaceuticals |
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