Exploratory IND studies: A review of Food and Drug Administration Guidance and similar provision in Europe

被引:3
作者
Attarchi, Faraneh [1 ]
机构
[1] Quintiles Inc, Global Regulatory Affairs, Regulatory Affairs Amer, Overland Pk, KS 66211 USA
来源
DRUG INFORMATION JOURNAL | 2007年 / 41卷 / 03期
关键词
exploratory IND; screening IND; microdose; critical path initiative; supporting toxicology; behavior;
D O I
10.1177/009286150704100303
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
In contrast to a traditional Investigational New Drug Application (IND), under which typically only one molecule can be investigated, an Exploratory IND provides a sponsor the opportunity to conduct early-stage clinical studies on a series of closely related molecules under the some IND. This provision, therefore, enables sponsors to select the most promising molecule, from a series of closely related molecules, for further development using human subjects. This article provides an overview of the advantages and limitations of this approach to drug development.
引用
收藏
页码:309 / 314
页数:6
相关论文
共 8 条
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