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Pharmaceutical Statistics|February 27, 2010
Proposed best practice for statisticians in the reporting and publication of pharmaceutical industry-sponsored clinical trialsJames Matcham, Steven Julious, Stephen Pyke, et al.Pharmaceutical Statistics|September 24, 2026
Testing Risk Difference of Two Proportions for Combined Unilateral and Bilateral DataJia Zhou, Chang-Xing MaPharmaceutical Statistics|September 13, 2026
Hierarchical Composite Endpoints for Dose Optimization in Early Phase Oncology TrialsYuxiang Wu, Xiaohan Guo, Ray Li, et al.Pharmaceutical Statistics|October 5, 2026
BOIN12-PFS: A Bayesian Optimal Interval Phase I/II Design Incorporating Progression-Free Survival EndpointYusuke Tanaka, Kentaro Takeda, Ryo Kitabayashi, et al.Pharmaceutical Statistics|August 26, 2026
Degrees-of-Freedom Approximations for Conditional-Mean Inference in Random-Lot Stability AnalysisAndrew T Karl, Heath Rushing, Richard K Burdick, et al.Pharmaceutical Statistics|September 30, 2026
TITE-LOCRM12: A Local Continual Reassessment Method for Drug Combination Optimization Based on Late-Onset Toxicity and Efficacy OutcomesLi Liu, Ruitao Lin, Nolan A WagesPageof 120