• 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

目前用于治疗萎缩性年龄相关性黄斑变性的药物和分子疗法:I 期至 III 期临床开发。

Current drug and molecular therapies for the treatment of atrophic age-related macular degeneration: phase I to phase III clinical development.

机构信息

a Department of Ophthalmology, The Second Xiangya Hospital , Central South University , Changsha , China.

b Department of Ophthalmology, The Hamilton Eye Institute , The University of Tennessee Health Science Center , Memphis , TN , USA.

出版信息

Expert Opin Investig Drugs. 2017 Oct;26(10):1103-1114. doi: 10.1080/13543784.2017.1369042. Epub 2017 Aug 24.

DOI:10.1080/13543784.2017.1369042
PMID:28816076
Abstract

Age-related macular degeneration (AMD) is the leading cause of vision loss among the elderly. Atrophic AMD, including early, intermediate and geographic atrophy (GA), accounts for ~90% of all cases. It is a multifactorial degeneration characterized by chronic inflammation, oxidative stress and aging components. Although no FDA-approved treatment yet exists for the late stage of atrophic AMD, multiple pathological mechanisms are partially known and several promising therapies are in various stages of development. Areas covered: Underlying mechanisms that define atrophic AMD will help provide novel therapeutic targets that will address this largely unmet clinical need. The purpose of this paper is to review current promising drugs that are being evaluated in clinical trials. Because no pharmacological treatments are currently available for late stage of atrophic AMD, any new therapy would have extensive market potential. Expert opinion: The number of AMD patients is predicted to increase to ~30 million worldwide by 2020. In response to this enormous unmet clinical need, new promising therapies are being developed and evaluated in clinical trials. We propose that the assessment of novel interventions will also need to consider the genotypes of participants, as the benefit may be determined by polymorphisms in an individual's genetic background.

摘要

年龄相关性黄斑变性(AMD)是老年人视力丧失的主要原因。萎缩性 AMD,包括早期、中期和地图状萎缩(GA),占所有病例的~90%。它是一种多因素变性,其特征为慢性炎症、氧化应激和衰老成分。尽管目前还没有 FDA 批准的治疗晚期萎缩性 AMD 的方法,但部分已知的多种病理机制和几种有前途的疗法正在不同阶段的开发中。

涵盖领域

定义萎缩性 AMD 的潜在机制将有助于提供新的治疗靶点,以满足这一主要未满足的临床需求。本文的目的是回顾正在临床试验中评估的当前有前途的药物。由于目前尚无治疗晚期萎缩性 AMD 的药物,任何新疗法都将具有广泛的市场潜力。

专家意见

预计到 2020 年,全球 AMD 患者人数将增加到~3000 万。为了应对这一巨大的未满足的临床需求,新的有前途的疗法正在临床试验中进行开发和评估。我们提出,对新干预措施的评估还需要考虑参与者的基因型,因为个体遗传背景中的多态性可能决定其获益。

相似文献

1
Current drug and molecular therapies for the treatment of atrophic age-related macular degeneration: phase I to phase III clinical development.目前用于治疗萎缩性年龄相关性黄斑变性的药物和分子疗法:I 期至 III 期临床开发。
Expert Opin Investig Drugs. 2017 Oct;26(10):1103-1114. doi: 10.1080/13543784.2017.1369042. Epub 2017 Aug 24.
2
Pharmacologic treatment of atrophic age-related macular degeneration.萎缩性年龄相关性黄斑变性的药物治疗。
Curr Opin Ophthalmol. 2010 May;21(3):190-6. doi: 10.1097/ICU.0b013e32833866c8.
3
Drugs in Phase II clinical trials for the treatment of age-related macular degeneration.用于治疗年龄相关性黄斑变性的处于II期临床试验阶段的药物。
Expert Opin Investig Drugs. 2015 Feb;24(2):183-99. doi: 10.1517/13543784.2015.961601. Epub 2014 Sep 22.
4
The genetics of age-related macular degeneration (AMD)--Novel targets for designing treatment options?年龄相关性黄斑变性(AMD)的遗传学——设计治疗方案的新靶点?
Eur J Pharm Biopharm. 2015 Sep;95(Pt B):194-202. doi: 10.1016/j.ejpb.2015.04.039. Epub 2015 May 16.
5
THE PATHOPHYSIOLOGY OF GEOGRAPHIC ATROPHY SECONDARY TO AGE-RELATED MACULAR DEGENERATION AND THE COMPLEMENT PATHWAY AS A THERAPEUTIC TARGET.年龄相关性黄斑变性继发地图样萎缩的病理生理学及作为治疗靶点的补体途径
Retina. 2017 May;37(5):819-835. doi: 10.1097/IAE.0000000000001392.
6
Investigational drugs in clinical trials for macular degeneration.用于治疗年龄相关性黄斑变性的临床试验中的研究性药物。
Expert Opin Investig Drugs. 2022 Oct;31(10):1067-1085. doi: 10.1080/13543784.2022.2113375. Epub 2022 Sep 20.
7
Investigational drugs inhibiting complement for the treatment of geographic atrophy.用于治疗地图状萎缩的抑制补体的研究性药物。
Expert Opin Investig Drugs. 2023 Jul-Dec;32(11):1009-1016. doi: 10.1080/13543784.2023.2276759. Epub 2023 Nov 24.
8
Dry Age-Related Macular Degeneration Pharmacology.干性年龄相关性黄斑变性药理学
Handb Exp Pharmacol. 2017;242:321-336. doi: 10.1007/164_2016_36.
9
New therapeutic targets in atrophic age-related macular degeneration.萎缩性年龄相关性黄斑变性的新治疗靶点
Expert Opin Ther Targets. 2007 May;11(5):625-39. doi: 10.1517/14728222.11.5.625.
10
Current therapeutic developments in atrophic age-related macular degeneration.萎缩性年龄相关性黄斑变性的当前治疗进展
Br J Ophthalmol. 2016 Jan;100(1):122-7. doi: 10.1136/bjophthalmol-2015-306972. Epub 2015 Nov 9.

引用本文的文献

1
Current Advancements in Mouse Models of Retinal Disease.视网膜疾病小鼠模型的最新进展。
Adv Exp Med Biol. 2023;1415:371-376. doi: 10.1007/978-3-031-27681-1_54.
2
Automatic geographic atrophy segmentation using optical attenuation in OCT scans with deep learning.利用深度学习通过光学衰减在光学相干断层扫描(OCT)中自动进行地理萎缩分割
Biomed Opt Express. 2022 Feb 7;13(3):1328-1343. doi: 10.1364/BOE.449314. eCollection 2022 Mar 1.
3
Optical Coherence Tomography Measurements of the Retinal Pigment Epithelium to Bruch Membrane Thickness Around Geographic Atrophy Correlate With Growth.
光学相干断层扫描测量视网膜色素上皮至脉络膜厚度与地理萎缩周围的生长相关。
Am J Ophthalmol. 2022 Apr;236:249-260. doi: 10.1016/j.ajo.2021.10.032. Epub 2021 Nov 13.
4
Age-Related Macular Degeneration: What Do We Know So Far?年龄相关性黄斑变性:我们目前了解多少?
Acta Med Litu. 2021;28(1):36-47. doi: 10.15388/Amed.2021.28.1.7. Epub 2021 Jan 18.
5
Interlink between Inflammation and Oxidative Stress in Age-Related Macular Degeneration: Role of Complement Factor H.年龄相关性黄斑变性中炎症与氧化应激的相互联系:补体因子H的作用
Biomedicines. 2021 Jun 30;9(7):763. doi: 10.3390/biomedicines9070763.
6
A Safe GDNF and GDNF/BDNF Controlled Delivery System Improves Migration in Human Retinal Pigment Epithelial Cells and Survival in Retinal Ganglion Cells: Potential Usefulness in Degenerative Retinal Pathologies.一种安全的胶质细胞源性神经营养因子(GDNF)和GDNF/脑源性神经营养因子(BDNF)控释系统可改善人视网膜色素上皮细胞的迁移及视网膜神经节细胞的存活:在视网膜退行性病变中的潜在应用价值
Pharmaceuticals (Basel). 2021 Jan 11;14(1):50. doi: 10.3390/ph14010050.
7
Ferroptosis drives photoreceptor degeneration in mice with defects in all-trans-retinal clearance.全反式视黄醛清除缺陷小鼠中,铁死亡驱动光感受器变性。
J Biol Chem. 2021 Jan-Jun;296:100187. doi: 10.1074/jbc.RA120.015779. Epub 2020 Dec 20.
8
The Role of Inflammation in Age-Related Macular Degeneration.炎症在年龄相关性黄斑变性中的作用。
Int J Biol Sci. 2020 Sep 23;16(15):2989-3001. doi: 10.7150/ijbs.49890. eCollection 2020.
9
Therapeutic Approaches with Intravitreal Injections in Geographic Atrophy Secondary to Age-Related Macular Degeneration: Current Drugs and Potential Molecules.与年龄相关性黄斑变性相关的地图状萎缩的玻璃体内注射治疗方法:现有药物和潜在分子。
Int J Mol Sci. 2019 Apr 4;20(7):1693. doi: 10.3390/ijms20071693.
10
Genetic screening for macular dystrophies in patients clinically diagnosed with dry age-related macular degeneration.对临床诊断为干性年龄相关性黄斑变性的患者进行黄斑营养不良的基因筛查。
Clin Genet. 2018 Dec;94(6):569-574. doi: 10.1111/cge.13447. Epub 2018 Oct 15.