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Pharmaceutical Statistics|March 28, 2020
A critical review of graphics for subgroup analyses in clinical trialsNicolás M Ballarini, Yi-Da Chiu, Franz König, et al.Pharmaceutical Statistics|March 29, 2020
Burden-of-illness vaccine efficacyAndrea Callegaro, Desmond Curran, Sean MatthewsPharmaceutical Statistics|November 28, 2009
Blinded sample size recalculation for clinical trials with normal data and baseline adjusted analysisTim Friede, Meinhard KieserPharmaceutical Statistics|October 20, 2025
Utility-Based Dose Optimization Approaches for Multiple-Dose Randomized Trial Designs Accounting for Multiple EndpointsGina D'Angelo, Guannan Chen, Di RanPharmaceutical Statistics|October 27, 2025
A Generalized Bayesian Hierarchical Model in Basket TrialsRuoxuan Xiang, John ScottPharmaceutical Statistics|September 27, 2025
Long-Term Safety Evaluations in the Presence of Switching: Evaluation of Two ApproachesSandra Schmeller, Rima Izem, Pedro Lopez Romero, et al.Pharmaceutical Statistics|June 24, 2025
Personalized Treatment Selection for Multivariate Ordinal Scale Outcomes and Multiple TreatmentsChathura Siriwardhana, Bakeerathan Gunaratnam, K B KulasekeraPharmaceutical Statistics|April 28, 2025
Why "Minimal Clinically Important Difference" for Interpreting the Magnitude of the Treatment Effect Is Not UsefulJitendra GanjuPharmaceutical Statistics|April 10, 2025
Control of Unconditional Type I Error in Clinical Trials With External Control Borrowing-A Two-Stage Adaptive Design PerspectivePing Gao, Xiao Ni, Jing Li, et al.Pharmaceutical Statistics|April 16, 2025
CUSUMIN Combination: A Cumulative Sum Interval Design for Phase I Cancer Drug-Combination TrialsTomoyoshi Hatayama, Seiichi YasuiPageof 120