Faricimab in the Treatment Landscape for Retinal Diseases: A Review

Anna K. Wu, David D Chong, Rishi P. Singh
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Abstract

Anti-vascular endothelial growth factor (anti-VEGF) injections are a mainstay of treatment for retinal vascular diseases such as neovascular age-related macular degeneration (nAMD), diabetic macular oedema (DMO) and retinal vein occlusion. While anti-VEGF monotherapy has helped improve visual outcomes in patients with these conditions, the need for frequent injections and follow-up visits, as well as the varying response to therapy are notable shortcomings. To address this, novel therapies have been investigated as adjuncts or alternatives to anti-VEGF monotherapy. One such therapy is faricimab, the first US Food and Drug Administration-approved intravitreal injection designed to target both VEGF-A and angiopoietin-Tie-2 for the treatment of nAMD and DMO. Clinical trial data thus far support that faricimab produces non-inferior visual and anatomical outcomes to standard anti-VEGF therapy, with longer durability, in these diseases. In this review, details regarding faricimab’s molecular development, clinical trial outcomes, and its prospect as the newest drug in the treatment landscape for retinal diseases will be discussed.
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法利昔单抗在视网膜疾病治疗中的应用综述
抗血管内皮生长因子(anti-VEGF)注射是治疗视网膜血管疾病的主要方法,如新生血管性年龄相关性黄斑变性(nAMD)、糖尿病性黄斑水肿(DMO)和视网膜静脉闭塞。虽然抗vegf单药治疗有助于改善这些疾病患者的视力,但需要频繁的注射和随访,以及对治疗的不同反应是明显的缺点。为了解决这个问题,已经研究了新的治疗方法作为抗vegf单药治疗的辅助或替代方法。其中一种治疗方法是faricimab,这是美国食品和药物管理局(fda)批准的第一种玻璃体内注射药物,旨在同时靶向VEGF-A和血管生成素-2,用于治疗nAMD和DMO。到目前为止,临床试验数据支持faricimab在这些疾病中产生的视觉和解剖结果不低于标准的抗vegf治疗,并且具有更长的持久性。本文将详细介绍法利昔单抗的分子开发、临床试验结果及其作为视网膜疾病治疗领域的最新药物的前景。
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