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Pharmaceutical Statistics|October 24, 2008
Using short-term evidence to predict six-month outcomes in clinical trials of signs and symptoms in rheumatoid arthritisRichard M Nixon, Nick Bansback, John W Stevens, et al.Pharmaceutical Statistics|January 24, 2007
A case study comparing a randomized withdrawal trial and a double-blind long-term trial for assessing the long-term efficacy of an antidepressantCraig Mallinckrodt, Christy Chuang-Stein, Paul McSorley, et al.Pharmaceutical Statistics|January 30, 2007
Nonparametric confidence intervals for Tmax in sequence-stratified crossover studiesSusan A Willavize, Elizabeth A MorgenthienPharmaceutical Statistics|May 17, 2007
Comparing two independent incidence rates using conditional and unconditional exact testsCong HanPharmaceutical Statistics|May 31, 2007
PREDICT-1 (CNA106030): the first powered, prospective trial of pharmacogenetic screening to reduce drug adverse eventsSara Hughes, Arlene Hughes, Cindy Brothers, et al.Pharmaceutical Statistics|November 4, 2006
Surrogate threshold effect: an alternative measure for meta-analytic surrogate endpoint validationTomasz Burzykowski, Marc BuysePharmaceutical Statistics|November 4, 2006
Comparison of models for average bioequivalence in replicated crossover designsSusan A Willavize, Elizabeth A MorgenthienPharmaceutical Statistics|November 4, 2006
Comparing proportional hazards and accelerated failure time models: an application in influenzaKatie Patel, Richard Kay, Lucy RowellPharmaceutical Statistics|November 4, 2006
Gatekeeping procedures in dose-response clinical trials based on the Dunnett testAlex Dmitrienko, Walt Offen, Ouhong Wang, et al.Pageof 119