Guidance on Preparing an Investigational New Drug Application for Fecal Microbiota Transplantation Studies

被引:63
作者
Kelly, Colleen R. [1 ]
Kunde, Sachin S. [2 ]
Khoruts, Alexander [3 ]
机构
[1] Brown Univ, Miriam Hosp, Alpert Sch Med, Womens Med Collaborat, Providence, RI USA
[2] Michigan State Univ, Helen DeVos Childrens Hosp, Grand Rapids, MI USA
[3] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
FDA; CBER; RECURRENT CLOSTRIDIUM-DIFFICILE; INFECTION;
D O I
10.1016/j.cgh.2013.09.060
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Fecal microbiota transplantation (FMT) is an effective treatment for Clostridium difficile infections that are refractory to antibiotic therapy. Because of the important roles of the microbiota in the function of the gastrointestinal tract and other aspects of human physiology, there is a growing interest in studying FMT for other clinical indications. The US Food and Drug Administration regulates clinical studies to evaluate the safety and efficacy of FMT. Studies of FMT for recurrent Clostridium difficile infection or other indications could require submission of an investigational new drug application. Most academic physicians and investigators do not have the regulatory experience necessary to undertake this process. We provide guidance to researchers on the preparation and submission of investigational new drug applications to study FMT.
引用
收藏
页码:283 / 288
页数:6
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