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Journal of Biopharmaceutical Statistics|April 25, 2013
An approximate approach to sampling size determination for the equivalence hypothesisChing-Ying Hsieh, Jen-Pei LiuJournal of Biopharmaceutical Statistics|April 25, 2013
Large sample tests for simultaneous comparison to multiple controls in terms of binomial proportionsJulia N Soulakova, Linlin LuoJournal of Biopharmaceutical Statistics|April 25, 2013
Approximating the baseline hazard function by taylor series for interval-censored time-to-event dataDing-Geng Chen, Lili Yu, Karl E Peace, et al.Journal of Biopharmaceutical Statistics|June 22, 2013
Bayesian sample size determination for a clinical trial with correlated continuous and binary outcomesJames D Stamey, Fanni Natanegara, John W SeamanJournal of Biopharmaceutical Statistics|June 22, 2013
Crossover versus parallel designs: dose-escalation design comparisons for first-in-human studiesZhiwu Yan, Balakrishna Hosmane, Charles LockeJournal of Biopharmaceutical Statistics|February 27, 2013
A threshold hazard model for estimating serious infection risk following anti-tumor necrosis factor therapy in rheumatoid arthritis patientsBo Fu, Mark Lunt, James Galloway, et al.Journal of Biopharmaceutical Statistics|July 12, 2014
Designing premarket observational comparative studies using existing data as controls: challenges and opportunitiesLilly Q Yue, Nelson Lu, Yunling XuJournal of Biopharmaceutical Statistics|October 22, 2013
Model-based estimates of long-term persistence of induced HPV antibodies: a flexible subject-specific approachMehreteab Aregay, Ziv Shkedy, Geert Molenberghs, et al.Journal of Biopharmaceutical Statistics|October 22, 2013
Evaluation of overall treatment effect in MMRMTao Song, Qunming Dong, Abdul J Sankoh, et al.Journal of Biopharmaceutical Statistics|October 22, 2013
Notes on testing noninferiority in ordinal data under the parallel groups designKung-Jong Lui, Kuang-Chao ChangPageof 216