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Pharmaceutical Statistics|July 12, 2024
Variable Duration Trial as an Alternative Design for Continuous EndpointsJitendra Ganju, Julie Guoguang MaPharmaceutical Statistics|December 18, 2025
Robust Modestly Weighted Log-Rank TestsDominic Magirr, Fredrik ÖhrnPharmaceutical Statistics|December 19, 2025
Informing the Borrowing Process for Dose-Finding Trials by Estimating the Similarity Between Population-Specific Dose-Toxicity CurvesDario Zocholl, Heiko Götte, Christina Habermehl, et al.Pharmaceutical Statistics|December 19, 2023
An evolutionary algorithm for the direct optimization of covariate balance between nonrandomized populationsStephen Privitera, Hooman Sedghamiz, Alexander Hartenstein, et al.Pharmaceutical Statistics|March 22, 2016
Estimands: discussion points from the PSI estimands and sensitivity expert groupAlan Phillips, Juan Abellan-Andres, Andersen Soren, et al.Pharmaceutical Statistics|July 7, 2018
Effect of heteroscedasticity between treatment groups on mixed-effects models for repeated measuresMasahiko Gosho, Kazushi MaruoPharmaceutical Statistics|December 22, 2019
Covariate adjustment for randomized controlled trials revisitedJixian WangPharmaceutical Statistics|September 7, 2020
Estimands in practice: Bridging the gap between study objectives and statistical analysisAlan Phillips, Tim ClarkPharmaceutical Statistics|January 14, 2021
Implementation of tripartite estimands using adherence causal estimators under the causal inference frameworkYongming Qu, Junxiang Luo, Stephen J RubergPharmaceutical Statistics|August 21, 2020
A method for sample size calculation via E-value in the planning of observational studiesYixin Fang, Weili He, Xiaofei Hu, et al.Pageof 119