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Pharmaceutical Statistics|September 18, 2014
A recommended analysis for 2 × 2 crossover trials with baseline measurementsDevan V MehrotraPharmaceutical Statistics|November 19, 2014
Estimation of group means when adjusting for covariates in generalized linear modelsYongming Qu, Junxiang LuoPharmaceutical Statistics|November 20, 2014
Likelihood approach for evaluating bioequivalence of highly variable drugsLiping Du, Leena ChoiPharmaceutical Statistics|August 24, 2017
Control-based imputation for sensitivity analyses in informative censoring for recurrent event dataFei Gao, Guanghan F Liu, Donglin Zeng, et al.Pharmaceutical Statistics|August 26, 2017
Competing risk analysis in a large cardiovascular clinical trial: An APEX substudyDouglas F Arbetter, Purva Jain, Megan K Yee, et al.Pharmaceutical Statistics|September 26, 2015
A Bayesian adaptive blinded sample size adjustment method for risk differencesAndrew Montgomery HartleyPharmaceutical Statistics|November 21, 2015
Practical guide to sample size calculations: an introductionLaura Flight, Steven A JuliousPharmaceutical Statistics|November 21, 2015
Practical guide to sample size calculations: superiority trialsLaura Flight, Steven A JuliousPharmaceutical Statistics|December 9, 2015
Continuous event monitoring via a Bayesian predictive approachJianing Di, Daniel Wang, H Robert Brashear, et al.Pharmaceutical Statistics|November 22, 2017
Design considerations in clinical trials with cure rate survival data: A case study in oncologySteven Sun, Grace Liu, Tianmeng Lyu, et al.Pageof 119