| Literature DB >> 24374152 |
Jorrit J Hornberg1, Morten Laursen1, Nina Brenden1, Mikael Persson1, Annemette V Thougaard1, Dorthe B Toft1, Tomas Mow2.
Abstract
In an effort to reduce toxicity-related attrition, different strategies have been implemented throughout the pharmaceutical industry. Previously (in Part I), we have outlined our 'integrated toxicology' strategy, which aims to provide timely go/no-go decisions (fail early) but also to show a direction to the drug discovery teams (showing what will not fail). In this review (Part II of the series) we describe our compound testing strategies with respect to cardiovascular safety, hepatotoxicity, genotoxicity, immunotoxicity and exploratory in vivo toxicity. We discuss the in vitro, ex vivo and in vivo assays and models we employ to assess safety risks and optimize compound series during the drug discovery process, including their predictivity and the decisions they generate.Entities:
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Year: 2013 PMID: 24374152 DOI: 10.1016/j.drudis.2013.12.009
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851