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Adaptive Clinical Trial Designs with Endpoint Selection and Sample Size Reassessment

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Endpoint selection and sample size reassessment for multiple binary endpoints based on blinded and/or unblinded data. Trial design that allows an adaptive modification of the primary endpoint based on blinded information obtained at an interim analysis. The decision rule chooses the endpoint with the lower estimated required sample size. Additionally, the sample size is reassessed using the estimated event probabilities and correlation between endpoints. The implemented design is proposed in Bofill Roig, M., Gómez Melis, G., Posch, M., and Koenig, F. (2022). doi:10.48550/arXiv.2206.09639.

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Version 1.1
Published 2023-02-03 451 days ago
Needs compilation? no
License MIT
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Maintainer

Maintainer

Marta Bofill Roig

marta.bofillroig@meduniwien.ac.at

Authors

Marta Bofill Roig

aut / cre

Guadalupe Gomez Melis

ctb

Franz Koenig

ctb

Martin Posch

ctb

Material

Reference manual
Package source

macOS

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arm64

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arm64

r-release

x86_64

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x86_64

Windows

r-develnot available

x86_64

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x86_64

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x86_64

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CompAREdesign