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Journal of Biopharmaceutical Statistics|June 11, 2014
Some challenges with statistical inference in adaptive designsH M James Hung, Sue-Jane Wang, Peiling YangPharmaceutical Statistics|August 11, 2007
Approaches to evaluation of treatment effect in randomized clinical trials with genomic subsetSue-Jane Wang, Robert T O'Neill, H M James HungPharmaceutical Statistics|September 28, 2010
Consideration of regional difference in design and analysis of multi-regional trialsH M James Hung, Sue-Jane Wang, Robert T O'NeillBiometrical Journal. Biometrische Zeitschrift|December 15, 2010
Impacts on type I error rate with inappropriate use of learn and confirm in confirmatory adaptive design trialsSue-Jane Wang, H M James Hung, Robert T O'NeillPharmaceutical Statistics|November 4, 2006
Adapting the sample size planning of a phase III trial based on phase II dataSue-Jane Wang, H M James Hung, Robert T O'NeillPharmaceutical Statistics|November 4, 2006
Methodological issues with adaptation of clinical trial designH M James Hung, Sue-Jane Wang, Robert T O'NeillBiometrical Journal. Biometrische Zeitschrift|April 10, 2009
Adaptive patient enrichment designs in therapeutic trialsSue-Jane Wang, H M James Hung, Robert T O'NeillContemporary Clinical Trials|May 2, 2017
A Bayesian interval dose-finding design addressingOckham's razor: mTPI-2Wentian Guo, Sue-Jane Wang, Shengjie Yang, et al.Journal of Biopharmaceutical Statistics|March 15, 2003
Statistical issues on objective, design, and analysis of noninferiority active-controlled clinical trialYi Tsong, Sue Jane Wang, H M James Hung, et al.Journal of Biopharmaceutical Statistics|July 19, 2005
Adaptive statistical analysis following sample size modification based on interim review of effect sizeH M James Hung, Lu Cui, Sue-Jane Wang, et al.Pageof 8