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Chooses subgroup specific optimal doses in a phase I dose finding clinical trial allowing for subgroup combination and simulates clinical trials under the subgroup specific time to event continual reassessment method. Chapple, A.G., Thall, P.F. (2018) <doi:10.1002/pst.1891>.
Package details |
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Author | Andrew Chapple |
Maintainer | Andrew Chapple <achapp@lsuhsc.edu> |
License | GPL-2 |
Version | 4.0.5 |
Package repository | View on CRAN |
Installation |
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