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145 | Mon, 8/10/2015, 8:30 AM - 10:20 AM | CC-617 | |
Adaptive Design II — Contributed Papers | |||
Biopharmaceutical Section | |||
Chair(s): Jimmy Hwang, UC San Francisco | |||
8:35 AM | A Practical Approach to Calculating Sample Size Based on Generalized Linear Models for Assessing Differential Expression Analysis in RNA-Seq Data — Chung-I Li, National Chiayi University | ||
8:50 AM | Intent-to-Treat Analysis for Longitudinal Studies with Dose Titration Scheme — Peter Zhang, Otsuka Pharmaceutical Development & Commercialization, Inc. ; Ye Yang, Otsuka Pharmaceutical Development & Commercialization, Inc. ; Xiaoshu Feng, Otsuka Pharmaceutical Development & Commercialization, Inc. | ||
9:05 AM | Meta-Analysis of Treatment-Biomarker Interaction in Randomized Clinical Trials — Shi Li | ||
9:20 AM | Confidence Interval Estimation for Number of Patient-Years Needed to Treat — Haiyuan Zhu, Actavis ; Xiao Wu, Actavis | ||
9:35 AM | Describing Patient-Reported Outcomes from Oncology Trials with Informative Dropouts Due to Adverse Events — Chia-Wen Ko, FDA ; Paul Kluetz, FDA ; Rajeshwari Sridhara, FDA | ||
10:05 AM | A Constrained Noninferiority Approach for Assessing Clinical Efficacy to Establish Biosimilarity — Jason Liao, Novartis Pharmaceuticals |
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