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Journal of Biopharmaceutical Statistics|January 22, 2013
Data mining for signal detection of adverse event safety dataHung-Chia Chen, Yi Tsong, James J ChenJournal of Biopharmaceutical Statistics|January 22, 2013
Automated method for detecting increases in frequency of spontaneous adverse event reports over timeWilliam DuMouchel, Nancy Yuen, Nassrin Payvandi, et al.Journal of Biopharmaceutical Statistics|January 22, 2013
Quantitative benefit-risk analysis for evaluating drug therapiesRalph L Kodell, James J ChenJournal of Biopharmaceutical Statistics|July 18, 2014
Sample size calculations for the development of biosimilar productsSeung-Ho Kang, Yongjo KimJournal of Biopharmaceutical Statistics|July 18, 2014
Equivalence assessment for interchangeability based on two-sided testsXiaoyu Dong, Yi TsongJournal of Biopharmaceutical Statistics|December 30, 2011
An estimation method of the clearance for a one-compartment model of a single bolus intravenous injection by a single samplingTakashi Funatogawa, Ikuko FunatogawaJournal of Biopharmaceutical Statistics|December 30, 2011
Simultaneous confidence bands for comparisons to placebo, with application to detecting the minimum effective doseJulia N Soulakova, Allan R Sampson, Gang Jia, et al.Journal of Biopharmaceutical Statistics|December 30, 2011
Interval estimation of the proportion ratio in repeated binary measurements under a stratified randomized clinical trial with noncomplianceKung-Jong Lui, Kuang-Chao ChangJournal of Biopharmaceutical Statistics|December 30, 2011
Optimal design of mixed-effects PK/PD models based on differential equationsYi Wang, Kent M Eskridge, Saralees NadarajahJournal of Biopharmaceutical Statistics|August 21, 2013
A note on partial covariate-adjustment and design considerations in noninferiority trials when patient-level data are not availableLei Nie, Guoxing Greg Soon, Karen Qi, et al.Pageof 219