Next-Generation Anti-IL-17 Agents for Psoriatic Disease: A Pipeline Review

被引:0
|
作者
Kim, Dahyeon [1 ]
Yang, Seanna [2 ]
Gill, Minka [3 ]
Babaei, Nickoulet [1 ]
Cervantes, Mireya [4 ]
Wu, Jashin J. [5 ]
机构
[1] Loma Linda Univ, Sch Med, Loma Linda, CA USA
[2] Tulane Univ, Sch Med, New Orleans, LA USA
[3] Indiana Univ, Sch Med, Indianapolis, IN USA
[4] Albany Med Coll, Albany, NY USA
[5] Univ Miami, Miller Sch Med, Dept Dermatol, 1600 NW 10th Ave,RMSB,Room 2023-A, Miami, FL 33136 USA
关键词
DOUBLE-BLIND; PLAQUE PSORIASIS; MULTICENTER; MODERATE; SAFETY; IZOKIBEP; EFFICACY;
D O I
10.1007/s40257-025-00928-w
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Innovations in biologics are transforming the treatment of psoriatic diseases. The ability to target specific levels of immune activation provides a distinct advantage. Interleukin (IL)-17 inhibitors fall into this class of biologics, and they are effectively used to treat a spectrum of psoriatic diseases, such as psoriasis vulgaris and psoriatic arthritis. In recent years, anti-IL-17 agents have been the focus of therapeutic development, with various formulations and routes of administration. In this manuscript, we review pipeline anti-IL-17 therapies for psoriatic diseases identified through a search of ClinicalTrials.gov (January 2019-December 2024) and other databases. Key agents under investigation include netakimab, vunakizumab, xeligekimab, gumokimab, HB0017, CJM 112, JS005, 608, LZM012, ZL-1102, izokibep, sonelokimab, DC-806, DC-853, and LEO 153339. Both preclinical and clinical trial data for each agent are summarized, with an emphasis on their efficacy, adverse effects, immunogenicity, and future outlooks.
引用
收藏
页码:307 / 320
页数:14
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