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首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >A global pharmaceutical company initiative: An evidence-based approach to define the upper limit of body weight loss in short term toxicity studies
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A global pharmaceutical company initiative: An evidence-based approach to define the upper limit of body weight loss in short term toxicity studies

机译:全球制药公司计划:一种基于证据的方法,用于定义短期毒性研究中体重减轻的上限

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摘要

Short term toxicity studies are conducted in animals to provide information on major adverse effects typically at the maximum tolerated dose (MTD). Such studies are important from a scientific and ethical perspective as they are used to make decisions on progression of potential candidate drugs, and to set dose levels for subsequent regulatory studies. The MTD is usually determined by parameters such as clinical signs, reductions in body weight and food consumption. However, these assessments are often subjective and there are no published criteria to guide the selection of an appropriate MTD. Even where an objective measurement exists, such as body weight loss (BWL), there is no agreement on what level constitutes an MTD. A global initiative including 15 companies, led by the National Centre for the Replacement, Refinement and Reduction of Animals in Research (NC3Rs), has shared data on BWL in toxicity studies to assess the impact on the animal and the study outcome. Information on 151 studies has been used to develop an alert/warning system for BWL in short term toxicity studies. The data analysis supports BWL limits for short term dosing (up to 7. days) of 10% for rat and dog and 6% for non-human primates (NHPs).
机译:在动物中进行了短期毒性研究,以提供通常在最大耐受剂量(MTD)下主要不良反应的信息。从科学和伦理的角度来看,此类研究非常重要,因为它们可用于确定潜在候选药物的进展并为后续的监管研究设定剂量水平。 MTD通常由临床症状,体重减轻和食物消耗等参数决定。但是,这些评估通常是主观的,没有公开的标准来指导适当的MTD的选择。即使在存在诸如体重减轻(BWL)之类的客观指标的情况下,也没有就什么水平构成MTD达成共识。由国家研究,替换和精制与减少动物研究中心(NC3Rs)牵头的一项由15家公司组成的全球计划,共享了毒性研究中有关BWL的数据,以评估对动物的影响和研究结果。在短期毒性研究中,已使用有关151个研究的信息来开发BWL的警报/警告系统。数据分析支持大鼠和狗的短期给药(最多7天)的BWL限值为10%,非人类灵长类动物(NHPs)的限值为6%。

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