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Journal of Biopharmaceutical Statistics|January 1, 1992
Alternative approaches to the analysis of binary and categorical repeated measurementsM G Kenward, B JonesJournal of Biopharmaceutical Statistics|January 1, 1992
Demonstration of the reproducibility of treatment efficacy from a single multicenter trialW J Huster, W C LouvJournal of Biopharmaceutical Statistics|November 9, 2010
Perspectives on the use of adaptive designs in clinical trials. Part I. Statistical considerations and issuesSue-Jane WangJournal of Biopharmaceutical Statistics|November 9, 2010
Viewpoints on the FDA draft adaptive designs guidance from the PhRMA working groupPaul Gallo, Keaven Anderson, Christy Chuang-Stein, et al.Journal of Biopharmaceutical Statistics|November 9, 2010
Review of draft FDA adaptive design guidanceThomas Cook, David L DeMetsJournal of Biopharmaceutical Statistics|November 9, 2010
Adaptive methods: telling "the rest of the story"Scott S Emerson, Thomas R FlemingJournal of Biopharmaceutical Statistics|December 31, 2010
An efficient algorithm to determine the optimal two-stage randomized multinomial designs in oncology clinical trialsYong Zhang, William Mietlowski, Bee Chen, et al.Journal of Biopharmaceutical Statistics|December 31, 2010
Estimating area under the curve and relative exposure in a pharmacokinetic study with data below quantification limitLiang Fang, Peng Chen, Chunlei Ke, et al.Journal of Biopharmaceutical Statistics|December 31, 2010
Statistical efficiency in multiple-to-one comparison trials with optimal allocation ratioJianliang Zhang, Jenny J ZhangJournal of Biopharmaceutical Statistics|March 11, 2011
Missing data in the regulation of medical devicesGregory Campbell, Gene Pennello, Lilly YuePageof 217