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Phase IV non-inferiority trials and additional claims of benefit

BACKGROUND: Non-inferiority (NI) trials in drug research are used to demonstrate that a new treatment is not less effective than an active comparator. Since phase IV trials typically aim at informing a clinical decision, the value of a phase IV non-inferiority trial hinges also on its clinical relev...

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Autores principales: Bernabe, Rosemarie DLC, Wangge, Grace, Knol, Mirjam J, Klungel, Olaf H, van Delden, Johannes JM, de Boer, Anthonius, Hoes, Arno W, Raaijmakers, Jan AM, van Thiel, Ghislaine JMW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679839/
https://www.ncbi.nlm.nih.gov/pubmed/23721202
http://dx.doi.org/10.1186/1471-2288-13-70
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author Bernabe, Rosemarie DLC
Wangge, Grace
Knol, Mirjam J
Klungel, Olaf H
van Delden, Johannes JM
de Boer, Anthonius
Hoes, Arno W
Raaijmakers, Jan AM
van Thiel, Ghislaine JMW
author_facet Bernabe, Rosemarie DLC
Wangge, Grace
Knol, Mirjam J
Klungel, Olaf H
van Delden, Johannes JM
de Boer, Anthonius
Hoes, Arno W
Raaijmakers, Jan AM
van Thiel, Ghislaine JMW
author_sort Bernabe, Rosemarie DLC
collection PubMed
description BACKGROUND: Non-inferiority (NI) trials in drug research are used to demonstrate that a new treatment is not less effective than an active comparator. Since phase IV trials typically aim at informing a clinical decision, the value of a phase IV non-inferiority trial hinges also on its clinical relevance. In such trials, clinical relevance would refer to the added benefit claims of a specific drug, apart from efficacy, relative to its comparator drug in the trial. METHODS: In this study, we reviewed 41 phase IV trials and extracted information on whether the authors mentioned any additional benefit beyond the NI (efficacy) claim of the drug and whether the additional benefit was proven in the trial. We checked whether the additional claim was based on descriptions only or on formal statistical analyses. RESULTS: Our results showed that 22 out of the 41 NI trials mentioned additional benefit of the test drug and most of these claims were related to the safety profile. Of all the post-authorization NI trials that claimed additional benefit, 10 out of 22 NI trials used formal statistical analyses to show additional benefit, and only one included a sample size calculation for the additional benefit prior to the trial. CONCLUSION: We conclude that there is room for improvement in terms of designing phase IV NI trials with added benefit claims and in proving these additional claims.
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spelling pubmed-36798392013-06-13 Phase IV non-inferiority trials and additional claims of benefit Bernabe, Rosemarie DLC Wangge, Grace Knol, Mirjam J Klungel, Olaf H van Delden, Johannes JM de Boer, Anthonius Hoes, Arno W Raaijmakers, Jan AM van Thiel, Ghislaine JMW BMC Med Res Methodol Research Article BACKGROUND: Non-inferiority (NI) trials in drug research are used to demonstrate that a new treatment is not less effective than an active comparator. Since phase IV trials typically aim at informing a clinical decision, the value of a phase IV non-inferiority trial hinges also on its clinical relevance. In such trials, clinical relevance would refer to the added benefit claims of a specific drug, apart from efficacy, relative to its comparator drug in the trial. METHODS: In this study, we reviewed 41 phase IV trials and extracted information on whether the authors mentioned any additional benefit beyond the NI (efficacy) claim of the drug and whether the additional benefit was proven in the trial. We checked whether the additional claim was based on descriptions only or on formal statistical analyses. RESULTS: Our results showed that 22 out of the 41 NI trials mentioned additional benefit of the test drug and most of these claims were related to the safety profile. Of all the post-authorization NI trials that claimed additional benefit, 10 out of 22 NI trials used formal statistical analyses to show additional benefit, and only one included a sample size calculation for the additional benefit prior to the trial. CONCLUSION: We conclude that there is room for improvement in terms of designing phase IV NI trials with added benefit claims and in proving these additional claims. BioMed Central 2013-05-30 /pmc/articles/PMC3679839/ /pubmed/23721202 http://dx.doi.org/10.1186/1471-2288-13-70 Text en Copyright © 2013 Bernabe et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bernabe, Rosemarie DLC
Wangge, Grace
Knol, Mirjam J
Klungel, Olaf H
van Delden, Johannes JM
de Boer, Anthonius
Hoes, Arno W
Raaijmakers, Jan AM
van Thiel, Ghislaine JMW
Phase IV non-inferiority trials and additional claims of benefit
title Phase IV non-inferiority trials and additional claims of benefit
title_full Phase IV non-inferiority trials and additional claims of benefit
title_fullStr Phase IV non-inferiority trials and additional claims of benefit
title_full_unstemmed Phase IV non-inferiority trials and additional claims of benefit
title_short Phase IV non-inferiority trials and additional claims of benefit
title_sort phase iv non-inferiority trials and additional claims of benefit
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679839/
https://www.ncbi.nlm.nih.gov/pubmed/23721202
http://dx.doi.org/10.1186/1471-2288-13-70
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