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Journal of Biopharmaceutical Statistics|November 9, 2010
On flexibility of adaptive designs and criteria for choosing a good one--a discussion of FDA draft guidanceBin Cheng, Shein-Chung Chow
Pharmaceutical Statistics|November 25, 2010
Assessing departure from dose linearity under a repeated measures incomplete block designBin Cheng, Shein-Chung Chow
Journal of Biopharmaceutical Statistics|February 18, 2020
Unified approaches to assessing treatment effect of traditional Chinese medicine based on health profilesBin Cheng, Bingzhi Zhang, Shein-Chung Chow
Journal of Biopharmaceutical Statistics|May 13, 2008
On power and sample size calculation for QT studies with recording replicates at given time pointShein-Chung Chow, Bin Cheng, Dennis Cosmatos
Journal of Biopharmaceutical Statistics|May 27, 2006
On the assessment of dose proportionality: a comparison of two slope approachesBin Cheng, Shein-Chung Chow, Wei-Lun Su
Journal of Biopharmaceutical Statistics|May 13, 2008
Statistical assessment of QT/QTc prolongation based on maximum of correlated normal random variablesBin Cheng, Shein-Chung Chow, David Burt, et al.
Wiley Interdisciplinary Reviews. Computational Statistics|September 13, 2014
Bioavailability and Bioequivalence in Drug DevelopmentShein-Chung Chow
Annual Review of Medicine|January 16, 2014
Adaptive clinical trial designShein-Chung Chow
Controlled Clinical Trials|October 24, 2002
A note on statistical methods for assessing therapeutic equivalenceShein-Chung Chow, Jun Shao
Journal of Biopharmaceutical Statistics|February 18, 2020
Innovative design and analysis for rare disease drug developmentShein-Chung Chow, Zhipeng Huang
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