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Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes

Two-stage designs are commonly used for Phase II trials. Optimal two-stage designs have the lowest expected sample size for a specific treatment effect, for example, the null value, but can perform poorly if the true treatment effect differs. Here we introduce a design for continuous treatment respo...

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Detalles Bibliográficos
Autores principales: Wason, James M. S., Mander, Adrian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662082/
https://www.ncbi.nlm.nih.gov/pubmed/22651118
http://dx.doi.org/10.1080/10543406.2010.528104
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author Wason, James M. S.
Mander, Adrian P.
author_facet Wason, James M. S.
Mander, Adrian P.
author_sort Wason, James M. S.
collection PubMed
description Two-stage designs are commonly used for Phase II trials. Optimal two-stage designs have the lowest expected sample size for a specific treatment effect, for example, the null value, but can perform poorly if the true treatment effect differs. Here we introduce a design for continuous treatment responses that minimizes the maximum expected sample size across all possible treatment effects. The proposed design performs well for a wider range of treatment effects and so is useful for Phase II trials. We compare the design to a previously used optimal design and show it has superior expected sample size properties.
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spelling pubmed-36620822013-05-28 Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes Wason, James M. S. Mander, Adrian P. J Biopharm Stat Research Article Two-stage designs are commonly used for Phase II trials. Optimal two-stage designs have the lowest expected sample size for a specific treatment effect, for example, the null value, but can perform poorly if the true treatment effect differs. Here we introduce a design for continuous treatment responses that minimizes the maximum expected sample size across all possible treatment effects. The proposed design performs well for a wider range of treatment effects and so is useful for Phase II trials. We compare the design to a previously used optimal design and show it has superior expected sample size properties. Taylor & Francis 2012-05-31 2012-07 /pmc/articles/PMC3662082/ /pubmed/22651118 http://dx.doi.org/10.1080/10543406.2010.528104 Text en Copyright © Taylor & Francis Group, LLC http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Taylor & Francis journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wason, James M. S.
Mander, Adrian P.
Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes
title Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes
title_full Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes
title_fullStr Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes
title_full_unstemmed Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes
title_short Minimizing the Maximum Expected Sample Size in Two-Stage Phase II Clinical Trials with Continuous Outcomes
title_sort minimizing the maximum expected sample size in two-stage phase ii clinical trials with continuous outcomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3662082/
https://www.ncbi.nlm.nih.gov/pubmed/22651118
http://dx.doi.org/10.1080/10543406.2010.528104
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