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Challenges for further successful development of tumor necrosis factor targeting therapies for uveitis

Authors
Thng, Zheng XianRegenold, JonathanBromeo, Albert JohnAkhavanrezayat, AmirThan, Ngoc T. T.Khatri, AnadiMohammadi, S. SaeedTran, Anh N. T.Shin, Yong UnKaraca, IrmakGhoraba, Hashem H.Or, Christopher Chi MongNguyen, Quan Dong
Issue Date
Feb-2024
Publisher
Ashley Publications Ltd.
Keywords
Adalimumab; autoimmune; biologics; corticosteroids; infliximab; noninfectious; tumor necrosis factor alpha inhibitor; uveitis
Citation
Expert Opinion on Investigational Drugs, v.33, no.2, pp 95 - 104
Pages
10
Indexed
SCIE
SCOPUS
Journal Title
Expert Opinion on Investigational Drugs
Volume
33
Number
2
Start Page
95
End Page
104
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197495
DOI
10.1080/13543784.2024.2311186
ISSN
1354-3784
1744-7658
Abstract
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-alpha (anti-TNF-alpha) agents have dramatically improved outcomes and changed treatment paradigms in NIU. Areas covered: The index article summarizes the present experience of anti-TNF-alpha agents in NIU pharmacotherapy and highlights the barriers to further research and development of anti-TNF-alpha agents for uveitis. Common challenges faced in NIU clinical drugs trials, specific difficulties in anti-TNF-alpha drug development, and promising competitor drug candidates are discussed and evaluated. Expert opinion: Anti-TNF-alpha 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-alpha 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-alpha drug development.
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