...
首页> 外文期刊>The Journal of Clinical Pharmacology: Official Journal of the American College of Clinical Pharmacology >Selection of the first-time dose in humans: comparison of different approaches based on interspecies scaling of clearance.
【24h】

Selection of the first-time dose in humans: comparison of different approaches based on interspecies scaling of clearance.

机译:在人类中首次剂量的选择:基于种间清除率的不同方法的比较。

获取原文
获取原文并翻译 | 示例
           

摘要

The authors describe four approaches to selecting a safe starting dose for humans in clinical drug trials based on interspecies scaling of clearance. Human clearance was predicted by scaling for 10 example drugs for which animal clearance values were available in the literature. The predicted human clearance values were then used to select the estimated starting dose in humans. These doses were then compared with the actual doses given to humans during clinical trials. All four approaches used to estimate the first-time dose in humans provided values that were within the dose range given to humans from Phases I to III. This work demonstrates that animal pharmacokinetic data can be used to estimate a suitable human starting dose, provided the data have been obtained from a dose that produces no adverse effects.
机译:作者描述了基于种间清除率缩放为临床药物试验选择人类安全起始剂量的四种方法。通过缩放10种示例药物来预测人类清除率,这些文献中有动物清除率值。然后将预测的人类清除率值用于选择人类的估计起始剂量。然后将这些剂量与临床试验中给予人类的实际剂量进行比较。用于估计人的首次剂量的所有四种方法所提供的值均在I至III期给予人的剂量范围内。这项工作证明,只要已从不会产生不利影响的剂量获得数据,就可以使用动物药代动力学数据来估算合适的人类起始剂量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号