• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

特发性肺纤维化的药物发现与开发:不断变化的格局。

Drug discovery and development in idiopathic pulmonary fibrosis: the changing landscape.

机构信息

TherapeutAix UG, Juttastrasse 18, 52066 Aachen, Germany.

TherapeutAix UG, Juttastrasse 18, 52066 Aachen, Germany.

出版信息

Drug Discov Today. 2024 Nov;29(11):104207. doi: 10.1016/j.drudis.2024.104207. Epub 2024 Oct 11.

DOI:10.1016/j.drudis.2024.104207
Abstract

Idiopathic pulmonary fibrosis (IPF) is an area of high unmet clinical need and high research activity in the pharmaceutical and biotech industries. The two approved therapies, nintedanib and pirfenidone, have issues with efficacy and tolerability. Despite a considerable number of development programs reaching late-stage Phase 2b or 3 clinical trials, no drug other than nintedanib and pirfenidone has successfully demonstrated a benefit for patients. An analysis of these failures, and consideration of the trajectories of some of the current development projects, may offer novel paradigms for choosing modes-of-action and for the development of successful drugs.

摘要

特发性肺纤维化(IPF)是制药和生物技术行业中一个高度未满足临床需求和高研究活跃度的领域。两种已批准的疗法,尼达尼布和吡非尼酮,在疗效和耐受性方面存在问题。尽管有相当数量的开发项目进入了后期的 2b 期或 3 期临床试验,但除了尼达尼布和吡非尼酮之外,没有其他药物成功证明对患者有益。对这些失败的分析,以及对一些当前开发项目轨迹的考虑,可能为选择作用模式和开发成功药物提供新的范例。

相似文献

1
Drug discovery and development in idiopathic pulmonary fibrosis: the changing landscape.特发性肺纤维化的药物发现与开发:不断变化的格局。
Drug Discov Today. 2024 Nov;29(11):104207. doi: 10.1016/j.drudis.2024.104207. Epub 2024 Oct 11.
2
Shedding light on developmental drugs for idiopathic pulmonary fibrosis.揭示特发性肺纤维化治疗药物的研发进展。
Expert Opin Investig Drugs. 2020 Aug;29(8):797-808. doi: 10.1080/13543784.2020.1782885. Epub 2020 Jun 24.
3
Efficacy of antifibrotic drugs, nintedanib and pirfenidone, in treatment of progressive pulmonary fibrosis in both idiopathic pulmonary fibrosis (IPF) and non-IPF: a systematic review and meta-analysis.抗纤维化药物尼达尼布和吡非尼酮治疗特发性肺纤维化(IPF)和非特发性肺纤维化(非 IPF)进展性肺纤维化的疗效:系统评价和荟萃分析。
BMC Pulm Med. 2021 Dec 11;21(1):411. doi: 10.1186/s12890-021-01783-1.
4
Emerging pharmacological options in the treatment of idiopathic pulmonary fibrosis (IPF).特发性肺纤维化(IPF)治疗中新兴的药理学选择。
Expert Rev Clin Pharmacol. 2024 Sep;17(9):817-835. doi: 10.1080/17512433.2024.2396121. Epub 2024 Aug 27.
5
Pirfenidone vs. nintedanib in patients with idiopathic pulmonary fibrosis: a retrospective cohort study.吡非尼酮对比尼达尼布治疗特发性肺纤维化患者的疗效:一项回顾性队列研究。
Respir Res. 2021 Oct 19;22(1):268. doi: 10.1186/s12931-021-01857-y.
6
Incidence of acute exacerbation of idiopathic pulmonary fibrosis in patients receiving antifibrotic agents: Real-world experience.接受抗纤维化药物治疗的特发性肺纤维化患者急性加重的发生率:真实世界经验。
Respir Med. 2021 Oct;187:106551. doi: 10.1016/j.rmed.2021.106551. Epub 2021 Jul 26.
7
Differential Discontinuation Profiles between Pirfenidone and Nintedanib in Patients with Idiopathic Pulmonary Fibrosis.特发性肺纤维化患者中吡非尼酮与尼达尼布之间的差异停药情况
Cells. 2022 Jan 2;11(1):143. doi: 10.3390/cells11010143.
8
Integrated bioinformatics analysis identifies established and novel TGFβ1-regulated genes modulated by anti-fibrotic drugs.综合生物信息学分析鉴定出 TGFβ1 调节的、受抗纤维化药物调控的已知和新基因。
Sci Rep. 2022 Feb 23;12(1):3080. doi: 10.1038/s41598-022-07151-1.
9
Pirfenidone and nintedanib exert additive antifibrotic effects by the SPP1-AKT pathway in macrophages and fibroblasts.吡非尼酮和尼达尼布通过 SPP1-AKT 通路在巨噬细胞和成纤维细胞中发挥相加抗纤维化作用。
Biochem Biophys Res Commun. 2024 Jul 5;716:150020. doi: 10.1016/j.bbrc.2024.150020. Epub 2024 Apr 26.
10
Idiopathic Pulmonary Fibrosis: Therapeutic Potential of Doxycycline, Pirfenidone, and Nintedanib, and the Role of Next-Generation Phenomics in Drug Discovery.特发性肺纤维化:强力霉素、吡非尼酮和尼达尼布的治疗潜力,以及下一代表型组学在药物发现中的作用。
OMICS. 2025 Mar;29(3):87-95. doi: 10.1089/omi.2024.0213. Epub 2025 Feb 3.

引用本文的文献

1
SIK2 Drives Pulmonary Fibrosis by Enhancing Fibroblast Glycolysis and Activation.SIK2通过增强成纤维细胞糖酵解和激活来驱动肺纤维化。
Biomedicines. 2025 Aug 6;13(8):1919. doi: 10.3390/biomedicines13081919.
2
Harnessing TP73‑targeted nintedanib: A novel strategy to halt triple‑negative breast cancer via p53‑PPARα/PI3K‑Akt pathway suppression.利用靶向TP73的尼达尼布:通过抑制p53-PPARα/PI3K-Akt通路阻止三阴性乳腺癌的新策略。
Int J Oncol. 2025 Nov;67(5). doi: 10.3892/ijo.2025.5794. Epub 2025 Aug 24.
3
Chest Imaging with a Collagen-Binding Probe-A Human Hydroxyproline Assay?
使用胶原结合探针进行胸部成像——一种人体羟脯氨酸检测方法?
Am J Respir Crit Care Med. 2025 Jul;211(7):1119-1120. doi: 10.1164/rccm.202503-0670ED.
4
Lamellarin D Acts as an Inhibitor of Type I Collagen Production.片螺素D可作为I型胶原蛋白生成的抑制剂。
ChemMedChem. 2025 May 5;20(9):e202401001. doi: 10.1002/cmdc.202401001. Epub 2025 Feb 10.
5
Hedgehog Signaling Pathway in Fibrosis and Targeted Therapies.纤维化中的刺猬信号通路及靶向治疗
Biomolecules. 2024 Nov 22;14(12):1485. doi: 10.3390/biom14121485.