Healthy Skepticism Library item: 14017
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Publication type: Journal Article
Robinson S, Delongeas JL, Donald E, Dreher D, Festag M, Kervyn S, Lampo A, Nahas K, Nogues V, Ockert D, Quinn K, Old S, Pickersgill N, Somers K, Stark C, Stei P, Waterson L, Chapman K.
A European pharmaceutical company initiative challenging the regulatory requirement for acute toxicity studies in pharmaceutical drug development.
Regul Toxicol Pharmacol 2008 Apr; 50:(3):345-52
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WPT-4R8WK2M-1&_user=10&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=c02db5bf494f34c077a7211a843b1ffb
Abstract:
Regulatory guidelines indicate acute toxicity studies in animals are considered necessary for pharmaceuticals intended for human use. This is the only study type where lethality is mentioned as an endpoint. The studies are carried out, usually in rodents, to support marketing of new drugs and to identify the minimum lethal dose. A European initiative including 18 companies has undertaken an evidence-based review of acute toxicity studies and assessed the value of the data generated. Preclinical and clinical information was shared on 74 compounds. The analysis indicated acute toxicity data was not used to (i) terminate drugs from development (ii) support dose selection for repeat dose studies in animals or (iii) to set doses in the first clinical trials in humans. The conclusion of the working group is that acute toxicity studies are not needed prior to first clinical trials in humans. Instead, information can be obtained from other studies, which are performed at more relevant doses for humans and are already an integral part of drug development. The conclusions have been discussed and agreed with representatives of regulatory bodies from the US, Japan and Europe.
sally.robinson@astrazeneca.com
Keywords:
MeSH Terms:
Animals
Clinical Trials as Topic
Computer Communication Networks
Data Collection
Dose-Response Relationship, Drug
Drug Industry/standards*
European Union
Humans
Legislation, Drug/standards*
Overdose
Pharmaceutical Preparations/standards*
Research Design
Toxicity Tests/standards*
Substances:
Pharmaceutical Preparations
Notes:
First available online 5 December 2007.
