进一步成功开发葡萄膜炎肿瘤坏死因子靶向疗法面临的挑战。

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Zheng Xian Thng, Jonathan Regenold, Albert John Bromeo, Amir Akhavanrezayat, Ngoc T T Than, Anadi Khatri, S Saeed Mohammadi, Anh N T Tran, Yong Un Shin, Irmak Karaca, Hashem H Ghoraba, Christopher Chi Mong Or, Quan Dong Nguyen
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引用次数: 0

摘要

导言:葡萄膜炎是以葡萄膜道炎症为特征的一类眼部疾病,是导致视力受损的主要原因之一。在发达国家,非感染性葡萄膜炎(NIU)占大多数病例,由于其严重性、慢性和高复发率,治疗具有挑战性。抗肿瘤坏死因子-α(anti-TNF-α)药物的出现大大改善了治疗效果,改变了非感染性葡萄膜炎的治疗模式:索引文章总结了抗肿瘤坏死因子-α药物在NIU药物治疗中的现有经验,并强调了进一步研究和开发用于葡萄膜炎的抗肿瘤坏死因子-α药物的障碍。专家意见:讨论并评估了NIU临床药物试验中面临的共同挑战、抗TNF-α药物开发中的具体困难以及有前景的候选竞争药物:抗肿瘤坏死因子-α药物彻底改变了非淋菌性尿道炎的药物治疗,大大提高了疗效,并具有良好的安全性。全身用药英夫利昔单抗和阿达木单抗在治疗非淋菌性尿道炎方面取得了巨大成功,但却没有推动这类药物的进一步发展。有人尝试在玻璃体内注射抗肿瘤坏死因子-α药物,但迄今为止尚未取得成功。随着专利到期、生物仿制药和更新、更新型分子的竞争,继续开发抗肿瘤坏死因子-α药物可能已不可行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenges for further successful development of tumor necrosis factor targeting therapies for uveitis.

Introduction: Uveitis is a heterogeneous group of ocular conditions characterized by inflammation of the uveal tract and is one of the leading causes of vision impairment. In developed countries, noninfectious uveitis (NIU) represents most cases and is challenging to treat due to its severity, chronicity, and high recurrence rates. The advent of anti-tumor necrosis factor-α (anti-TNF-α) agents have dramatically improved outcomes and changed treatment paradigms in NIU.

Areas covered: The index article summarizes the present experience of anti-TNF-α agents in NIU pharmacotherapy and highlights the barriers to further research and development of anti-TNF-α agents for uveitis. Common challenges faced in NIU clinical drugs trials, specific difficulties in anti-TNF-α drug development, and promising competitor drug candidates are discussed and evaluated.

Expert opinion: Anti-TNF-α agents have revolutionized NIU pharmacotherapy and greatly improved outcomes with good safety profiles. The great success of systemic infliximab and adalimumab in NIU treatment has resulted in little impetus for further development of this class of medication. Attempts have been made to deliver anti-TNF-α agents intravitreally but that has not been successful thus far. With expiring patents, competition from biosimilars and newer, novel molecules, it may not be viable to continue pursuing anti-TNF-α drug development.

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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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