患有炎症性肠病的儿童因目前的药物批准政策而处于不利地位:呼吁紧急改变。

IF 1.8 Q3 GASTROENTEROLOGY & HEPATOLOGY
Crohn's & Colitis 360 Pub Date : 2025-06-19 eCollection Date: 2025-04-01 DOI:10.1093/crocol/otaf036
Benjamin Sahn, Ross M Maltz, Joel R Rosh
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引用次数: 0

摘要

由于缺乏美国食品和药物管理局批准的生物和小分子药物,儿童炎症性肠病(IBD)的治疗受到严重阻碍。本综述解释了儿童IBD患者因这一问题而面临的负担,并评估了成人和儿童IBD患者在药物批准方面的显著历史时间差异。作者随后深入关注了与风湿病免疫介导性疾病儿童相比,IBD儿童获批治疗的明显差异,强调了用于获得风湿病儿童药物批准的证据严格程度的差异。这篇社论最后呼吁改变监管机构的方案,采用一种现代化的战略,加快批准治疗IBD儿童的先进疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Children With Inflammatory Bowel Diseases are Disadvantaged by Current Drug Approval Policies: A Call for Urgent Change.

Treatment of pediatric inflammatory bowel disease (IBD) is significantly hindered by the lack of US Food and Drug Administration-approved biologic and small-molecule medications. This review explains the burdens faced by children with IBD because of this problem and appraises the marked historical timeline differences in medication approval between adults and children with IBD. The authors follow with an in-depth focus on the pointed disparity in approved therapies for children with IBD compared to children with rheumatologic immune-mediated diseases, highlighting the differences in stringency of evidence that has been used to gain medication approval for children with rheumatologic diseases. The editorial concludes with a call for change in regulatory agency protocols, to adopt a modernized strategy that will expedite the approval of advanced therapies for children with IBD.

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来源期刊
Crohn's & Colitis 360
Crohn's & Colitis 360 Medicine-Gastroenterology
CiteScore
2.50
自引率
0.00%
发文量
41
审稿时长
12 weeks
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