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Biometrics|January 24, 2018
A utility-based design for randomized comparative trials with ordinal outcomes and prognostic subgroupsThomas A Murray, Ying Yuan, Peter F Thall, et al.
Statistics in Medicine|May 15, 2024
Design and sample size determination for multiple-dose randomized phase II trials for dose optimizationPeng Yang, Daniel Li, Ruitao Lin, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 18, 2018
Time-to-Event Bayesian Optimal Interval Design to Accelerate Phase I TrialsYing Yuan, Ruitao Lin, Daniel Li, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 17, 2026
Generalised pairwise comparisons in dose-optimisation oncology trials: beyond safety to multi-outcome dose selectionEmily Alger, Ruitao Lin, J Jack Lee, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 6, 2025
Practical Considerations for Using the TITE-BOIN Design to Handle Late-onset Toxicity or Fast Accrual in Phase I TrialsKai Chen, Ting-Yu Chen, Yiming Zhang, et al.
Statistics in Medicine|November 5, 2024
Bayesian Safety and Futility Monitoring in Phase II Trials Using One Utility-Based RuleJuhee Lee, Peter F Thall
JCO Clinical Cancer Informatics|January 13, 2021
BOIN Suite: A Software Platform to Design and Implement Novel Early-Phase Clinical TrialsYanhong Zhou, Ruitao Lin, Ying-Wei Kuo, et al.
Journal of the Royal Statistical Society. Series C, Applied Statistics|September 10, 2013
Evaluating Joint Effects of Induction-Salvage Treatment Regimes on Overall Survival in Acute LeukemiaAbdus S Wahed, Peter F Thall
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