A Unified Decision Framework for Phase I Dose-Finding Designs
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry, Genetics and Molecular Biology (miscellaneous),Statistics and Probability
Link
https://link.springer.com/content/pdf/10.1007/s12561-023-09379-5.pdf
Reference20 articles.
1. Storer Barry E (1989) Design and analysis of phase I clinical trials. Biometrics 1989:925–937
2. Liu M, Wang SJ, Ji Y (2020) The i3+ 3 design for phase I clinical trials. J Biopharm Stat 30(2):294–304
3. John O, Margaret P, Lloyd F (1990) Continual reassessment method: a practical design for phase 1 clinical trials in cancer. Biometrics 1990:33–48
4. Neuenschwander B, Branson M, Gsponer T (2008) Critical aspects of the Bayesian approach to phase I cancer trials. Stat Med 27(13):2420–2439
5. Mourad T, André R (2010) Dose finding with escalation with overdose control (EWOC) in cancer clinical trials. Stat Sci 2010:217–226
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