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Pharmaceutical Statistics|November 17, 2025
A Unified Approach to Covariate Adjustment for Survival Endpoints in Randomized Clinical TrialsZhiwei Zhang, Ya Wang, Dong XiPharmaceutical Statistics|November 18, 2025
Quantile Effect on Duration of Response: A Zero-Inflated Censored Regression ApproachNan Sun, Jixian Wang, Ram TiwariPharmaceutical Statistics|February 7, 2025
Estimation of the Restricted Mean Duration of Response (RMDoR) in OncologyAntonios Daletzakis, Kit C B Roes, Marianne A JonkerPharmaceutical Statistics|February 5, 2025
Estimating the Strength of Binding Affinity via Delta-Delta-G for Hit Screening After a Deming Regression CalibrationKanaka Tatikola, Javier CabreraPharmaceutical Statistics|December 12, 2023
Analysis of two binomial proportions in noninferiority confirmatory trialsHassan Lakkis, Andrew LakkisPharmaceutical Statistics|December 26, 2023
Evaluation of a flexible piecewise linear mixed-effects model in the analysis of randomized cross-over trialsMoses Mwangi, Geert Verbeke, Edmund Njeru Njagi, et al.Pharmaceutical Statistics|December 28, 2023
Sample size calculation for mixture model based on geometric average hazard ratio and its applications to nonproportional hazardZixing Wang, Qingyang Zhang, Allen Xue, et al.Pharmaceutical Statistics|September 24, 2024
Quality by Design for Preclinical In Vitro Assay DevelopmentJonathan Jones, Bairu Zhang, Xiang Zhang, et al.Pharmaceutical Statistics|March 5, 2024
A propensity score-integrated approach for leveraging external data in a randomized controlled trial with time-to-event endpointsWei-Chen Chen, Nelson Lu, Chenguang Wang, et al.Pharmaceutical Statistics|February 28, 2024
What they forgot to tell you about machine learning with an application to pharmaceutical manufacturingKjell Johnson, Max KuhnPageof 120