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Journal of Biopharmaceutical Statistics|June 22, 2013
The joint modeling of drug and positive control effects to estimate sample size and power in crossover "thorough" QT/QTc studiesBalakrishna Hosmane, Charles Locke, Yi-Lin ChiuJournal of Biopharmaceutical Statistics|June 2, 2012
Flexible analytical methods for adding a treatment arm mid-study to an ongoing clinical trialJordan J Elm, Yuko Y Palesch, Gary G Koch, et al.Journal of Biopharmaceutical Statistics|June 2, 2012
Analysis of time-to-event data with nonuniform patient entry and loss to follow-up under a two-stage seamless adaptive design with weibull distributionQingshu Lu, Siu-Keung Tse, Shein-Chung Chow, et al.Journal of Biopharmaceutical Statistics|June 2, 2012
Sample size estimation in single-arm clinical trials with multiple testing under frequentist and Bayesian approachesBoris G Zaslavsky, John ScottJournal of Biopharmaceutical Statistics|June 2, 2012
Minimizing the maximum expected sample size in two-stage Phase II clinical trials with continuous outcomesJames M S Wason, Adrian P ManderJournal of Biopharmaceutical Statistics|June 2, 2012
Optimization of adaptive designs: efficiency evaluationSandeep Menon, Mark ChangJournal of Biopharmaceutical Statistics|September 1, 1993
Statistical considerations for cross-sectional data relating to tracheal reconstruction over timeJ S Preisser, G G Koch, W W ShockleyJournal of Biopharmaceutical Statistics|September 1, 1993
Statistical estimates and clinical trialsL E BraitmanJournal of Biopharmaceutical Statistics|September 1, 1993
Confidence intervals and controlled clinical trials: incompatible tools for medical researchD B HallJournal of Biopharmaceutical Statistics|August 26, 2000
Simultaneous testing strategy for comparing two treatments in a stratified binomial trialR A Railkar, D V Mehrotra, B IglewiczPageof 216