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Applications and Case Studies

Bayesian Model Averaging Continual Reassessment Method in Phase I Clinical Trials

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Pages 954-968 | Received 01 Aug 2008, Published online: 01 Jan 2012

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Read on this site (16)

Ziqing Wang, Jingyi Zhang, Tian Xia, Ruyue He & Fangrong Yan. (2023) A Bayesian phase I–II clinical trial design to find the biological optimal dose on drug combination. Journal of Biopharmaceutical Statistics 0:0, pages 1-14.
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Takashi Asakawa, Akihiro Hirakawa & Chikuma Hamada. (2014) Bayesian Model Averaging Continual Reassessment Method for Bivariate Binary Efficacy and Toxicity Outcomes in Phase I Oncology Trials. Journal of Biopharmaceutical Statistics 24:2, pages 310-325.
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Jin Zhang & ThomasM. Braun. (2013) A Phase I Bayesian Adaptive Design to Simultaneously Optimize Dose and Schedule Assignments Both Between and Within Patients. Journal of the American Statistical Association 108:503, pages 892-901.
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Guosheng Yin, Shurong Zheng & Jiajing Xu. (2013) Fractional Dose-Finding Methods with Late-Onset Toxicity in Phase I Clinical Trials. Journal of Biopharmaceutical Statistics 23:4, pages 856-870.
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Ying Yuan & Guosheng Yin. (2011) Robust EM Continual Reassessment Method in Oncology Dose Finding. Journal of the American Statistical Association 106:495, pages 818-831.
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