Shields Melissa K, Ferreira Lisia Barros, Ali Syed B, Dedina Liana, Lim Lyndell L, Suhler Eric B, Smith Justine R
College of Medicine and Public Health, and Flinders Health and Medical Research Institute, Flinders University, Adelaide, South Australia, Australia.
Centro de Medicina Humanizado, Curitiba, Paraná, Brazil.
J Ophthalmic Inflamm Infect. 2025 Jun 5;15(1):49. doi: 10.1186/s12348-025-00502-9.
Non-infectious uveitis is an uncommon eye condition, but an important cause of substantial vision impairment and blindness around the world. An individualized treatment approach may include corticosteroids, conventional immunomodulatory medications, and biologic immunomodulatory agents, delivered locally to the eye or by systemic routes.
In this narrative review, we describe pivotal phase III clinical trials that have provided the information guiding clinical practice in non-infectious uveitis today, focusing on studies of injected or surgically positioned local therapeutics, systemic immunomodulatory drugs, and the combination of both. We report on design, outcome measures, and key effectiveness and safety results of these trials. We also describe selected phase III clinical trials that are presently in progress, with results expected within the coming approximately 3 years. Finally, we summarize the state of the field and speculate on fruitful areas of research and development for new phase III clinical trials of drugs to treat non-infectious uveitis.
The locally delivered therapeutics for non-infectious uveitis that have been studied in phase III clinical trials are largely corticosteroid-based. Trials have shown these locally placed corticosteroids to be effective, with complications that include elevated intraocular pressure and cataract. A minority of systemic immunomodulatory drugs used to treat non-infectious uveitis have been studied in phase III clinical trials. Key information obtained from those trials includes the following: similar effectiveness of methotrexate and mycophenolate mofetil for uveitis involving the posterior eye; usefulness of interferon-beta for intermediate uveitis; and potent anti-inflammatory activity of adalimumab in recalcitrant uveitis. Phase III clinical trials of immunomodulatory drugs with novel targets or routes of delivery can be anticipated in the foreseeable future. Interest in defining treatments for specific subsets of non-infectious uveitis through phase III clinical trials is also likely. For productive cross-referencing of clinical trial results, we recommend the use of core outcome measures.
非感染性葡萄膜炎是一种罕见的眼部疾病,但在全球范围内是导致严重视力损害和失明的重要原因。个体化治疗方法可能包括局部或全身应用皮质类固醇、传统免疫调节药物和生物免疫调节药物。
在本叙述性综述中,我们描述了关键的III期临床试验,这些试验为当今非感染性葡萄膜炎的临床实践提供了指导信息,重点关注注射或手术定位的局部治疗、全身免疫调节药物以及两者联合应用的研究。我们报告了这些试验的设计、结局指标以及关键的有效性和安全性结果。我们还描述了目前正在进行的部分III期临床试验,预计在未来约3年内得出结果。最后,我们总结了该领域的现状,并推测了治疗非感染性葡萄膜炎新药III期临床试验的富有成效的研发领域。
在III期临床试验中研究的用于非感染性葡萄膜炎的局部给药疗法主要基于皮质类固醇。试验表明,这些局部应用的皮质类固醇有效,但并发症包括眼压升高和白内障。用于治疗非感染性葡萄膜炎的少数全身免疫调节药物已在III期临床试验中进行了研究。从这些试验中获得的关键信息包括:甲氨蝶呤和霉酚酸酯对累及后段眼的葡萄膜炎疗效相似;干扰素-β对中间葡萄膜炎有用;阿达木单抗在顽固性葡萄膜炎中具有强大的抗炎活性。在可预见的未来,可以预期针对具有新靶点或给药途径的免疫调节药物进行III期临床试验。通过III期临床试验确定非感染性葡萄膜炎特定亚组治疗方法的兴趣也可能存在。为了有效地交叉引用临床试验结果,我们建议使用核心结局指标。