Article(id=1291339235294961901, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291339070622396983, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2025.03.030, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1724083200000, receivedDateStr=2024-08-20, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785808865616, onlineDateStr=2026-08-04, pubDate=1739721600000, pubDateStr=2025-02-17, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785808865616, onlineIssueDateStr=2026-08-04, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785808865616, creator=13041195026, updateTime=1785808865616, updator=13041195026, issue=Issue{id=1291339070622396983, tenantId=1146029695717560320, journalId=1246415772164075586, year='2025', volume='41', issue='3', pageStart='301', pageEnd='450', issueExtLink='null', onlineDate='null', pubDate='1739721600000', pubDateStr='2025-02-17', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785808826353, creator='13041195026', updateTime=1785808826353, updator='13041195026', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=445, endPage=450, ext={EN=ArticleExt(id=1291339236209320174, articleId=1291339235294961901, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=Research and consideration on regulatory strategies for fecal microbiota products in different countries, columnId=1291339025546211579, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Drug Evaluation and Administration, runingTitle=null, highlight=null, articleAbstract=

In recent years, fecal microbiota for transplantation (FMT) has developed rapidly as a potential intervention for numerous conditions that may be caused by gut microbiota disorders and there are fecal microbiota products (FMP) have been approved to treat recurrent Clostridioides difficile infection (rCDI). There is currently no unified positioning and regulatory measures for FMP internationally, which poses challenges for the development of such products. This article proposes several thoughts on the regulation and evaluation of FMP based on reviewing the regulatory strategies of different countries for FMP and the research and regulatory situation of approved products, in order to provide reference for the development and application of such products.

, authors=Hua-jing YIN1, Yi-fei CHEN2, 3, Mao-shan YIN1, Tao SUN1, authorsList=Hua-jing YIN, Yi-fei CHEN, Mao-shan YIN, Tao SUN, authorCompany=null, correspAuthors=Tao SUN, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1291339236997849327, articleId=1291339235294961901, tenantId=1146029695717560320, journalId=1246415772164075586, language=CN, title=不同国家粪菌产品的监管策略研究及思考, columnId=1291339025730760957, journalTitle=中国临床药理学杂志, columnName=药物评价与管理, runingTitle=null, highlight=null, articleAbstract=

近年来,粪菌移植(FMT)作为新的治疗手段发展迅速,正被开发用于治疗肠道微生物群紊乱可能导致的多种不同的疾病,且已有粪菌产品(FMP)获批上市用于治疗复发性艰难梭菌感染(rCDI)。目前国际上对FMP尚无统一的定位和监管措施,为此类产品的开发带来挑战。本文通过梳理不同国家对FMP的监管策略和已上市产品的研究、监管情况,提出对FMP监管和评价的几点思考,以期为此类产品的研发和应用提供参考。

, authors=尹华静1, 陈一飞2, 3, 尹茂山1, 孙涛1, authorsList=尹华静, 陈一飞, 尹茂山, 孙涛, authorCompany=null, correspAuthors=孙涛, authorNote=

尹华静(1989-),女,副主任药师,主要从事药品非临床技术审评工作

, correspAuthorsNote=
孙涛,主任药师 Tel: (010)88096607 E-mail:
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不同国家粪菌产品的监管策略研究及思考
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尹华静 1 , 陈一飞 2, 3 , 尹茂山 1 , 孙涛 1
中国临床药理学杂志 | 药物评价与管理 2025,41(3): 445-450
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中国临床药理学杂志 |药物评价与管理 2025 , 41 (3) : 445 -450
不同国家粪菌产品的监管策略研究及思考
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尹华静1, 陈一飞2, 3, 尹茂山1, 孙涛1
作者信息
  • 1.国家药品监督管理局 药品审评中心,北京 100076
  • 2.上海药品审评核查中心 创新与监管科学发展部,上海 201210
  • 3.华东师范大学-上海药品审评核查中心 药品监管科学联合研究中心,上海 201210
通讯作者:
孙涛,主任药师 Tel: (010)88096607 E-mail:
作者简介:

尹华静(1989-),女,副主任药师,主要从事药品非临床技术审评工作

Research and consideration on regulatory strategies for fecal microbiota products in different countries
Hua-jing YIN1, Yi-fei CHEN2, 3, Mao-shan YIN1, Tao SUN1
Affiliations
  • 1.Center for Drug Evaluation, National Medical Products Administration, Beijing 100076, China
  • 2.Innovation and Regulatory Science Development Department, Shanghai Center for Drug Evaluation and Inspection, Shanghai 201210, China
  • 3.ECNU-SCDEI Collaborative Research Center for Drug Regulatory Science, Shanghai 201210, China
出版时间: 2025-02-17 doi: 10.13699/j.cnki.1001-6821.2025.03.030
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近年来,粪菌移植(FMT)作为新的治疗手段发展迅速,正被开发用于治疗肠道微生物群紊乱可能导致的多种不同的疾病,且已有粪菌产品(FMP)获批上市用于治疗复发性艰难梭菌感染(rCDI)。目前国际上对FMP尚无统一的定位和监管措施,为此类产品的开发带来挑战。本文通过梳理不同国家对FMP的监管策略和已上市产品的研究、监管情况,提出对FMP监管和评价的几点思考,以期为此类产品的研发和应用提供参考。

粪菌移植  /  药品监管  /  活生物制剂

In recent years, fecal microbiota for transplantation (FMT) has developed rapidly as a potential intervention for numerous conditions that may be caused by gut microbiota disorders and there are fecal microbiota products (FMP) have been approved to treat recurrent Clostridioides difficile infection (rCDI). There is currently no unified positioning and regulatory measures for FMP internationally, which poses challenges for the development of such products. This article proposes several thoughts on the regulation and evaluation of FMP based on reviewing the regulatory strategies of different countries for FMP and the research and regulatory situation of approved products, in order to provide reference for the development and application of such products.

fecal microbiota for transplantation  /  drug administration  /  live biotherapeutic product
尹华静, 陈一飞, 尹茂山, 孙涛. 不同国家粪菌产品的监管策略研究及思考. 中国临床药理学杂志, 2025 , 41 (3) : 445 -450 . DOI: 10.13699/j.cnki.1001-6821.2025.03.030
Hua-jing YIN, Yi-fei CHEN, Mao-shan YIN, Tao SUN. Research and consideration on regulatory strategies for fecal microbiota products in different countries[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (3) : 445 -450 . DOI: 10.13699/j.cnki.1001-6821.2025.03.030

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2025年第41卷第3期
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doi: 10.13699/j.cnki.1001-6821.2025.03.030
  • 接收时间:2024-08-20
  • 首发时间:2026-08-04
  • 出版时间:2025-02-17
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  • 收稿日期:2024-08-20
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    1.国家药品监督管理局 药品审评中心,北京 100076
    2.上海药品审评核查中心 创新与监管科学发展部,上海 201210
    3.华东师范大学-上海药品审评核查中心 药品监管科学联合研究中心,上海 201210

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孙涛,主任药师 Tel: (010)88096607 E-mail:
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https://castjournals.cast.org.cn/joweb/zglcylxzz/CN/10.13699/j.cnki.1001-6821.2025.03.030
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2种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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