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Journal of Biopharmaceutical Statistics|August 21, 2013
An analytical approach to assess the predictive value of biomarkers in Phase II decision makingStavros Nikolakopoulos, Willem M van der Wal, Kit C B RoesJournal of Biopharmaceutical Statistics|August 21, 2013
An adaptive two-stage dose-response design method for establishing proof of conceptYoko Franchetti, Stewart J Anderson, Allan R SampsonJournal of Biopharmaceutical Statistics|August 7, 2015
Bayesian methods for the design and analysis of noninferiority trialsMargaret Gamalo-Siebers, Aijun Gao, Mani Lakshminarayanan, et al.Journal of Biopharmaceutical Statistics|August 7, 2015
Optimal design of perturbations for individual two-compartment pharmacokinetic analysisMatthew S Shotwell, Minchun Zhou, William H FissellJournal of Biopharmaceutical Statistics|August 7, 2015
Mixture-based gatekeeping procedures for multiplicity problems with multiple sequences of hypothesesAlex Dmitrienko, George Kordzakhia, Thomas BrechenmacherJournal of Biopharmaceutical Statistics|August 8, 2015
Avoiding ambiguity with the Type I error rate in noninferiority trialsSeung-Ho KangJournal of Biopharmaceutical Statistics|September 23, 2015
A simulation study of nonparametric total deviation index as a measure of agreement based on quantile regressionLawrence Lin, Yi Pan, A S Hedayat, et al.Journal of Biopharmaceutical Statistics|September 24, 2015
Making what's advanced today routine tomorrowStephen J RubergJournal of Biopharmaceutical Statistics|September 25, 2015
Selecting the primary endpoint in a randomized clinical trial: The ARE methodOleguer Plana-Ripoll, Guadalupe GómezJournal of Biopharmaceutical Statistics|February 17, 2016
Interim decision-making strategies in adaptive designs for population selection using time-to-event endpointsRyuji Uozumi, Chikuma HamadaPageof 216