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Journal of Biopharmaceutical Statistics|August 29, 2019
Approximate confidence limit for the reference scaled bioequivalence with a parallel designJason J Z Liao, Yifang LiJournal of Biopharmaceutical Statistics|February 28, 2019
Profile clustering in clinical trials with longitudinal and functional data methodsHangjun Gong, Xiaolei Xun, Yingchun ZhouJournal of Biopharmaceutical Statistics|October 9, 2019
Homogeneity assessment for pivotal medical device clinical studiesXu Yan, Chul Ahn, Jianxiong Chu, et al.Journal of Biopharmaceutical Statistics|March 11, 2011
Defining, evaluating, and removing bias induced by linear imputation in longitudinal clinical trials with MNAR missing dataRonald W Helms, Laura Helms Reece, Russell W Helms, et al.Journal of Biopharmaceutical Statistics|March 11, 2011
Intent-to-randomize corrections for missing data resulting from run-in selection bias in clinical trials for chronic conditionsVance W Berger, Behrang ValiJournal of Biopharmaceutical Statistics|March 11, 2011
Analysis of missing mechanism in IVUS imaging clinical trials with missing covariatesMingxiu Hu, Tianyue ZhouJournal of Biopharmaceutical Statistics|March 11, 2011
Handling missing data in vaccine clinical trials for immunogenicity and safety evaluationXiaoming Li, William W B Wang, Guanghan F Liu, et al.Journal of Biopharmaceutical Statistics|March 29, 2011
Optimal serial dilutions designs for drug discovery experimentsAlexander N Donev, Randall D TobiasJournal of Biopharmaceutical Statistics|March 29, 2011
The adjustment of the type I error rate in noninferiority trials with λ-margin approach: each of two different new drugs is approved with two independent trials with the same active controlSeung-Ho Kang, Yuman RyuJournal of Biopharmaceutical Statistics|March 29, 2011
Estimators and confidence intervals for the proportion using binary auxiliary information with applications to pharmaceutical studiesM Rueda, J F Muñoz, A Arcos, et al.Pageof 216