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Journal of Biopharmaceutical Statistics|August 21, 2013
Evaluating and adjusting for premature censoring of progression-free survivalMark Rothmann, Kallappa Koti, Kyung Yul Lee, et al.Journal of Biopharmaceutical Statistics|August 21, 2013
A comparison of bias-corrected covariance estimators for generalized estimating equationsChunpeng Fan, Donghui Zhang, Cun-Hui ZhangJournal of Biopharmaceutical Statistics|February 20, 2016
Multiple contrast type tests for the evaluation of animal carcinogenicity studiesMohammad Rahman, Ram TiwariJournal of Biopharmaceutical Statistics|February 20, 2016
Group-sequential three-arm noninferiority clinical trial designsToshimitsu Ochiai, Toshimitsu Hamasaki, Scott R Evans, et al.Journal of Biopharmaceutical Statistics|February 17, 2016
Sample size determination with familywise control of both type I and type II errors in clinical trialsBushi Wang, Naitee TingJournal of Biopharmaceutical Statistics|February 17, 2016
Novel dose-finding designs and considerations on practical implementations in oncology clinical trialsBo Huang, Paul Bycott, Enayet TalukderJournal of Biopharmaceutical Statistics|March 5, 2016
Sample size determination for fold-increase endpoints defined by paired interval-censored dataYing Xu, K F Lam, Yin Bun CheungJournal of Biopharmaceutical Statistics|October 22, 2013
Dose-time-response modeling using negative binomial distributionMunmun Roy, Kanak Choudhury, M M Islam, et al.Journal of Biopharmaceutical Statistics|October 22, 2013
Selection of hypothesis weights and ordering when testing multiple hypotheses in clinical trialsBrian L Wiens, Alex Dmitrienko, Olga MarchenkoJournal of Biopharmaceutical Statistics|June 14, 2016
Power and sample size calculation for the additive hazard modelPei-Fang SuPageof 218