Cancer phase I trial design using drug combinations when a fraction of dose limiting toxicities is attributable to one or more agents
DOI10.1002/BIMJ.201700166zbMath1419.62373arXiv1709.00918OpenAlexW2751316271WikidataQ64957294 ScholiaQ64957294MaRDI QIDQ4967095
J. L. Jiménez, Mourad Tighiouart, Mauro Gasparini
Publication date: 2 July 2019
Published in: Biometrical Journal (Search for Journal in Brave)
Full work available at URL: https://arxiv.org/abs/1709.00918
continual reassessment methoddrug combinationcancer phase I trialsattributable toxicitycopula type models
Applications of statistics to biology and medical sciences; meta analysis (62P10) Bayesian inference (62F15) Characterization and structure theory for multivariate probability distributions; copulas (62H05)
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