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Review of dose setting for the extended one-generation reproductive toxicity studies (OECD TG 443): Considerations on ECHA's dose level selection recommendations.
Beekhuijzen, Manon; Richmond, Emily; Manton, Jason; Coder, Pragati S; Goyak, Katy; Ghaffari, Rashin; Makris, Susan L; Van Cruchten, Steven; Zorrilla, Leah; Mitchell-Ryan, Shermaine.
Afiliação
  • Beekhuijzen M; Charles River Laboratories, 's-Hertogenbosch, the Netherlands.
  • Richmond E; Exponent International Ltd., Harrogate, United Kingdom.
  • Manton J; Exponent International Ltd., Harrogate, United Kingdom.
  • Coder PS; Charles River Laboratories Ashland LLC, Ashland, OH, 44805, USA.
  • Goyak K; ExxonMobil Biomedical Sciences, Inc., Annandale, NJ, 08801, USA.
  • Ghaffari R; Corteva Agriscience, Newark, DE, 19711, USA.
  • Makris SL; Office of Research and Development, Center for Public Health and Environmental Assessment, US Environmental Protection Agency (retired), Washington, DC, 20460, USA.
  • Van Cruchten S; Comparative Perinatal Development (CoPeD), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Antwerp, Belgium.
  • Zorrilla L; Bayer Crop Science, 700 Chesterfield Parkway West, Chesterfield, MO, 63017, USA.
  • Mitchell-Ryan S; Health and Environmental Sciences Institute (HESI), Washington, DC, 20005, USA. Electronic address: smitchell-ryan@hesiglobal.org.
Regul Toxicol Pharmacol ; 151: 105665, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38885874
ABSTRACT
During 2020, The European Chemicals Agency (ECHA) began evaluating the OECD Test Guideline 443 Extended One Generation Reproductive Toxicity Study (EOGRTS) to analyze specific aspects related to study design, conduct and toxicological findings. A significant outcome of this ECHA evaluation focused on adequate dose level selection. Subsequently, ECHA published recommendations for DART studies, however, these recommendations seemingly do not align with the principles of the 3Rs, animal welfare or human safety goals, specifically, regarding three aspects. First, the requirement to segregate testing for sexual function and fertility from the ability to produce normally developing offspring increases the risk of inadequate identification of postnatal hazards for development and sexual function and fertility, therefore failing human health protection goals. Second, the current ECHA high-dose level setting recommendations for EOGRTS exceed the MTD (Maximum Tolerated Dose), and therefore compromise the interpretation of the biological response relative to the intrinsic effect of the chemical under evaluation. Third, the combination of these aspects will result in an increase in the number of animals tested, increasing animal welfare concerns. This paper reflects the consensus of subject matter experts, professional, and scientific societies who have authored and signed on to this statement. The signatories encourage ECHA to adopt a revised science-driven approach to the dose selection criteria that strikes a balance between regulatory vigilance and scientific pragmatism.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reprodução / Testes de Toxicidade / Relação Dose-Resposta a Droga Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Reprodução / Testes de Toxicidade / Relação Dose-Resposta a Droga Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article