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Pharmaceutical Statistics|February 13, 2014
Analysis of safety data in clinical trials using a recurrent event approachQi Gong, Barbara Tong, Alexander Strasak, et al.Pharmaceutical Statistics|April 3, 2008
Missing item imputation for quality-of-life instruments with application to asthma quality-of-life questionnairesJixian Wang, Guenter Rapatz, Adam Lowy, et al.Pharmaceutical Statistics|October 27, 2018
Lessons from meta-analyses of randomized clinical trials for analysis of distributed networks of observational databasesAndrew Bate, Christy Chuang-Stein, Andrew Roddam, et al.Pharmaceutical Statistics|October 30, 2018
Strategies for composite estimands in confirmatory clinical trials: Examples from trials in nasal polyps and steroid reductionOliver N KeenePharmaceutical Statistics|March 7, 2019
Statistical testing strategies for assessing treatment efficacy and marker accuracy in phase III trialsTakahiro Nonaka, Masataka Igeta, Shigeyuki MatsuiPharmaceutical Statistics|April 5, 2017
Enabling robust assessment of QTc prolongation in early phase clinical trialsDevan V Mehrotra, Li Fan, Fang Liu, et al.Pharmaceutical Statistics|October 13, 2016
Response-adaptive clinical trials: case studies in the medical literatureAndrew P GrievePharmaceutical Statistics|September 30, 2016
Some practical considerations in three-arm non-inferiority trial designMing Zhou, Sudeep KunduPharmaceutical Statistics|August 16, 2016
Trimmed means for symptom trials with dropoutsThomas Permutt, Feng LiPharmaceutical Statistics|February 13, 2026
Handling Missing Data in Participants with Baseline but No Post-Baseline DataCraig Mallinckrodt, Ilya Lipkovich, Samuel Dickson, et al.Pageof 119