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Publisher: Taylor and Francis Ltd

Volume 19, Number 4, July 2009

On Assessing Bioequivalence Using Genomic Data with Model Misspecification
pp. 571-579(9)
Authors: Lu, Qingshu; Tse, Siu-Keung; Chow, Shein-Chung; Yang, Jun

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Sample Size Allocation to Regions in a Multiregional Trial
pp. 580-594(15)
Author: Uesaka, Hiroyuki

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A Seamless Phase II/III Design with Sample-Size Re-Estimation
pp. 595-609(15)
Authors: Bischoff, Wolfgang; Miller, Frank

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Two Confidence Interval Approaches on the Dependability Coefficient in a Two-Factor Crossed Design
pp. 610-624(15)
Authors: Ting, Naitee; Cappelleri, Joseph; Bushmakin, Andrew

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Design and Sample Size for Evaluating Combinations of Drugs of Linear and Loglinear Dose-Response Curves
pp. 625-640(16)
Authors: Fang, Hong-Bin; Tian, Guo-Liang; Li, Wei; Tan, Ming

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Drug-Drug Interaction Prediction Assessment
pp. 641-657(17)
Authors: Zhou, Jihao; Qin, Zhaohui; Sara, Quinney; Kim, Seongho; Wang, Zhiping; Hall, Stephen; Li, Lang

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A Transition Model for Ordinal Response Data with Random Dropout: An Application to the Fluvoxamine Data
pp. 658-671(14)
Authors: Ghahroodi, Z. Rezaei; Ganjali, M.; Berridge, D.

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Baseline Observation Carry Forward: Reasoning, Properties, and Practical Issues
pp. 672-684(13)
Authors: Shao, Jun; Jordan, David; Pritchett, Yili

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Optimal Two-Stage Designs Allowing Flexibility in Number of Subjects for Phase II Clinical Trials
pp. 721-731(11)
Authors: Masaki, Nobuyuki; Koyama, Tatsuki; Yoshimura, Isao; Hamada, Chikuma

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Parametric Modeling of Localized Melanoma Prognosis and Outcome
pp. 732-747(16)
Authors: Ding, Shouluan; Soong, Seng-Jaw; Lin, Hui-Yi; Desmond, Renee; Balch, Charles

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