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Industry perspectives on biomarker qualification
Biomarkers have the potential to expedite drug development, increase patient safety, and optimize clinical response. Yet few have achieved regulatory qualification. A survey was conducted to clarify industry's perspective on biomarker qualification and identify the most promising biomarkers for...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065241/ https://www.ncbi.nlm.nih.gov/pubmed/26378777 http://dx.doi.org/10.1002/cpt.264 |
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author | Lavezzari, G Womack, AW |
author_facet | Lavezzari, G Womack, AW |
author_sort | Lavezzari, G |
collection | PubMed |
description | Biomarkers have the potential to expedite drug development, increase patient safety, and optimize clinical response. Yet few have achieved regulatory qualification. A survey was conducted to clarify industry's perspective on biomarker qualification and identify the most promising biomarkers for drug development. The results across toxicities/clinical areas highlight challenges in regulatory qualification, although early prioritization and alignment on an evidentiary standard framework are key factors in facilitating biomarker development and qualification. |
format | Online Article Text |
id | pubmed-5065241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50652412016-10-25 Industry perspectives on biomarker qualification Lavezzari, G Womack, AW Clin Pharmacol Ther Reviews Biomarkers have the potential to expedite drug development, increase patient safety, and optimize clinical response. Yet few have achieved regulatory qualification. A survey was conducted to clarify industry's perspective on biomarker qualification and identify the most promising biomarkers for drug development. The results across toxicities/clinical areas highlight challenges in regulatory qualification, although early prioritization and alignment on an evidentiary standard framework are key factors in facilitating biomarker development and qualification. John Wiley and Sons Inc. 2015-10-22 2016-02 /pmc/articles/PMC5065241/ /pubmed/26378777 http://dx.doi.org/10.1002/cpt.264 Text en © 2015 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics. This is an open access article under the terms of the Creative Commons Attribution‐NoDerivs (http://creativecommons.org/licenses/by-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited and no modifications or adaptations are made. |
spellingShingle | Reviews Lavezzari, G Womack, AW Industry perspectives on biomarker qualification |
title | Industry perspectives on biomarker qualification |
title_full | Industry perspectives on biomarker qualification |
title_fullStr | Industry perspectives on biomarker qualification |
title_full_unstemmed | Industry perspectives on biomarker qualification |
title_short | Industry perspectives on biomarker qualification |
title_sort | industry perspectives on biomarker qualification |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065241/ https://www.ncbi.nlm.nih.gov/pubmed/26378777 http://dx.doi.org/10.1002/cpt.264 |
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