糖尿病视网膜病变的未来治疗:正在开发的药物治疗产品

M. Stewart
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引用次数: 5

摘要

糖尿病性黄斑水肿(DMO)是导致老年人视力丧失的主要原因。几十年来,黄斑激光光凝是DMO的主要治疗方法,但最近已被玻璃体内注射皮质类固醇和抑制血管内皮生长因子(VEGF)作用的药物所取代。在III期试验中,抗vegf药物将最佳矫正视力平均提高了+12个字母,但高达40%的患者对治疗的反应不理想。新的抗vegf药物abicipar和brolucizumab可能在III期新生血管性年龄相关性黄斑变性试验中具有延长的作用时间,DMO试验正在计划中。血管生成素-2抑制剂,无论是作为抗vegf药物的联合制剂,还是作为双特异性抗体,都在DMO的II期试验中。刺激Tie2受体的药物通过皮下注射给药。静脉注射的抗体,如tocilizumab和teprotumumab,可以降低糖尿病介导的炎症,正在进入早期研究阶段。其他外用(甲胺)和口服(米诺环素)给药途径的药物正在开发中。其中一些药物可能在未来5-10年内可供患者使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future Treatments of Diabetic Retinopathy: Pharmacotherapeutic Products Under Development
Diabetic macular oedema (DMO) is the leading cause of vision loss in working aged individuals. Macular laser photocoagulation was the primary DMO treatment for several decades, but has recently been replaced by intravitreal injections of corticosteroids and drugs that inhibit the actions of vascular endothelial growth factor (VEGF). In Phase III trials, anti-VEGF drugs improve best corrected visual acuity by a mean of +12 letters, but up to 40% of patients have sub-optimal responses to therapy. The new anti-VEGF drugs abicipar and brolucizumab may possess extended durations of action in Phase III neovascular age-related macular degeneration trials, and DMO trials are being planned. Angiopoietin-2 inhibitors, both as co-formulations with anti-VEGF drugs and as bispecific antibodies, are in Phase II trials for DMO. Drugs that stimulate the Tie2 receptor are administered via subcutaneous injections. Intravenously administered antibodies that decrease diabetes-mediated inflammation, such as tocilizumab and teprotumumab, are entering early phase studies. Other drugs with topical (mecamylamine) and oral (minocycline) delivery routes are being developed. Several of these drugs may become available to patients within the next 5–10 years.
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