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Pharmaceutical Statistics|June 21, 2012
A proof-of-concept clinical trial design combined with dose-ranging explorationXin Wang, Naitee TingPharmaceutical Statistics|January 30, 2010
Effects of unstratified and centre-stratified randomization in multi-centre clinical trialsVladimir V AnisimovPharmaceutical Statistics|April 9, 2019
A generalized Bayesian nonlinear mixed-effects regression model for zero-inflated longitudinal count data in tuberculosis trialsDivan Aristo Burger, Robert Schall, Rianne Jacobs, et al.Pharmaceutical Statistics|July 17, 2022
Left truncation in linked data: A practical guide to understanding left truncation and applying it using SAS and RYanling Jin, Thanh G N Ton, Devin Incerti, et al.Pharmaceutical Statistics|May 8, 2023
A comparative study of adaptive trial designs for dose optimizationJingyi Zhang, Xin Chen, Bosheng Li, et al.Pharmaceutical Statistics|April 25, 2023
Time-to-event calibration-free odds design: A robust efficient design for phase I trials with late-onset outcomesHuaqing Jin, Guosheng YinPharmaceutical Statistics|April 1, 2021
Improving sample size recalculation in adaptive clinical trials by resamplingCarolin Herrmann, Corinna Kluge, Maximilian Pilz, et al.Pharmaceutical Statistics|October 13, 2012
A generalisation of T-optimality for discriminating between competing models with an application to pharmacokinetic studiesPavan Vajjah, Stephen B DuffullPharmaceutical Statistics|July 6, 2025
A General Approach for Sample Size Calculation With Nonproportional Hazards and Cure RatesHuan Cheng, Xiaoyun Li, Jianghua HePharmaceutical Statistics|September 14, 2025
Prediction Intervals for Overdispersed Binomial Endpoints and Their Application to Toxicological Historical Control DataMax Menssen, Jonathan RathjensPageof 119