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Value of shared preclinical safety studies – The eTOX database

A first analysis of a database of shared preclinical safety data for 1214 small molecule drugs and drug candidates extracted from 3970 reports donated by thirteen pharmaceutical companies for the eTOX project (www.etoxproject.eu) is presented. Species, duration of exposure and administration route d...

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Autores principales: Briggs, Katharine, Barber, Chris, Cases, Montserrat, Marc, Philippe, Steger-Hartmann, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598263/
https://www.ncbi.nlm.nih.gov/pubmed/28962354
http://dx.doi.org/10.1016/j.toxrep.2014.12.004
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author Briggs, Katharine
Barber, Chris
Cases, Montserrat
Marc, Philippe
Steger-Hartmann, Thomas
author_facet Briggs, Katharine
Barber, Chris
Cases, Montserrat
Marc, Philippe
Steger-Hartmann, Thomas
author_sort Briggs, Katharine
collection PubMed
description A first analysis of a database of shared preclinical safety data for 1214 small molecule drugs and drug candidates extracted from 3970 reports donated by thirteen pharmaceutical companies for the eTOX project (www.etoxproject.eu) is presented. Species, duration of exposure and administration route data were analysed to assess if large enough subsets of homogenous data are available for building in silico predictive models. Prevalence of treatment related effects for the different types of findings recorded were analysed. The eTOX ontology was used to determine the most common treatment-related clinical chemistry and histopathology findings reported in the database. The data were then mined to evaluate sensitivity of established in vivo biomarkers for liver toxicity risk assessment. The value of the database to inform other drug development projects during early drug development is illustrated by a case study.
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spelling pubmed-55982632017-09-28 Value of shared preclinical safety studies – The eTOX database Briggs, Katharine Barber, Chris Cases, Montserrat Marc, Philippe Steger-Hartmann, Thomas Toxicol Rep Article A first analysis of a database of shared preclinical safety data for 1214 small molecule drugs and drug candidates extracted from 3970 reports donated by thirteen pharmaceutical companies for the eTOX project (www.etoxproject.eu) is presented. Species, duration of exposure and administration route data were analysed to assess if large enough subsets of homogenous data are available for building in silico predictive models. Prevalence of treatment related effects for the different types of findings recorded were analysed. The eTOX ontology was used to determine the most common treatment-related clinical chemistry and histopathology findings reported in the database. The data were then mined to evaluate sensitivity of established in vivo biomarkers for liver toxicity risk assessment. The value of the database to inform other drug development projects during early drug development is illustrated by a case study. Elsevier 2014-12-18 /pmc/articles/PMC5598263/ /pubmed/28962354 http://dx.doi.org/10.1016/j.toxrep.2014.12.004 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Briggs, Katharine
Barber, Chris
Cases, Montserrat
Marc, Philippe
Steger-Hartmann, Thomas
Value of shared preclinical safety studies – The eTOX database
title Value of shared preclinical safety studies – The eTOX database
title_full Value of shared preclinical safety studies – The eTOX database
title_fullStr Value of shared preclinical safety studies – The eTOX database
title_full_unstemmed Value of shared preclinical safety studies – The eTOX database
title_short Value of shared preclinical safety studies – The eTOX database
title_sort value of shared preclinical safety studies – the etox database
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598263/
https://www.ncbi.nlm.nih.gov/pubmed/28962354
http://dx.doi.org/10.1016/j.toxrep.2014.12.004
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