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The evolving role of investigative toxicology in the pharmaceutical industry
For decades, preclinical toxicology was essentially a descriptive discipline in which treatment-related effects were carefully reported and used as a basis to calculate safety margins for drug candidates. In recent years, however, technological advances have increasingly enabled researchers to gain...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924869/ https://www.ncbi.nlm.nih.gov/pubmed/36781957 http://dx.doi.org/10.1038/s41573-022-00633-x |
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author | Pognan, Francois Beilmann, Mario Boonen, Harrie C. M. Czich, Andreas Dear, Gordon Hewitt, Philip Mow, Tomas Oinonen, Teija Roth, Adrian Steger-Hartmann, Thomas Valentin, Jean-Pierre Van Goethem, Freddy Weaver, Richard J. Newham, Peter |
author_facet | Pognan, Francois Beilmann, Mario Boonen, Harrie C. M. Czich, Andreas Dear, Gordon Hewitt, Philip Mow, Tomas Oinonen, Teija Roth, Adrian Steger-Hartmann, Thomas Valentin, Jean-Pierre Van Goethem, Freddy Weaver, Richard J. Newham, Peter |
author_sort | Pognan, Francois |
collection | PubMed |
description | For decades, preclinical toxicology was essentially a descriptive discipline in which treatment-related effects were carefully reported and used as a basis to calculate safety margins for drug candidates. In recent years, however, technological advances have increasingly enabled researchers to gain insights into toxicity mechanisms, supporting greater understanding of species relevance and translatability to humans, prediction of safety events, mitigation of side effects and development of safety biomarkers. Consequently, investigative (or mechanistic) toxicology has been gaining momentum and is now a key capability in the pharmaceutical industry. Here, we provide an overview of the current status of the field using case studies and discuss the potential impact of ongoing technological developments, based on a survey of investigative toxicologists from 14 European-based medium-sized to large pharmaceutical companies. |
format | Online Article Text |
id | pubmed-9924869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99248692023-02-14 The evolving role of investigative toxicology in the pharmaceutical industry Pognan, Francois Beilmann, Mario Boonen, Harrie C. M. Czich, Andreas Dear, Gordon Hewitt, Philip Mow, Tomas Oinonen, Teija Roth, Adrian Steger-Hartmann, Thomas Valentin, Jean-Pierre Van Goethem, Freddy Weaver, Richard J. Newham, Peter Nat Rev Drug Discov Perspective For decades, preclinical toxicology was essentially a descriptive discipline in which treatment-related effects were carefully reported and used as a basis to calculate safety margins for drug candidates. In recent years, however, technological advances have increasingly enabled researchers to gain insights into toxicity mechanisms, supporting greater understanding of species relevance and translatability to humans, prediction of safety events, mitigation of side effects and development of safety biomarkers. Consequently, investigative (or mechanistic) toxicology has been gaining momentum and is now a key capability in the pharmaceutical industry. Here, we provide an overview of the current status of the field using case studies and discuss the potential impact of ongoing technological developments, based on a survey of investigative toxicologists from 14 European-based medium-sized to large pharmaceutical companies. Nature Publishing Group UK 2023-02-13 2023 /pmc/articles/PMC9924869/ /pubmed/36781957 http://dx.doi.org/10.1038/s41573-022-00633-x Text en © Springer Nature Limited 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Perspective Pognan, Francois Beilmann, Mario Boonen, Harrie C. M. Czich, Andreas Dear, Gordon Hewitt, Philip Mow, Tomas Oinonen, Teija Roth, Adrian Steger-Hartmann, Thomas Valentin, Jean-Pierre Van Goethem, Freddy Weaver, Richard J. Newham, Peter The evolving role of investigative toxicology in the pharmaceutical industry |
title | The evolving role of investigative toxicology in the pharmaceutical industry |
title_full | The evolving role of investigative toxicology in the pharmaceutical industry |
title_fullStr | The evolving role of investigative toxicology in the pharmaceutical industry |
title_full_unstemmed | The evolving role of investigative toxicology in the pharmaceutical industry |
title_short | The evolving role of investigative toxicology in the pharmaceutical industry |
title_sort | evolving role of investigative toxicology in the pharmaceutical industry |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9924869/ https://www.ncbi.nlm.nih.gov/pubmed/36781957 http://dx.doi.org/10.1038/s41573-022-00633-x |
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