黄斑变性
医学
脉络膜新生血管
血管内皮生长因子
贝伐单抗
补体系统
新生血管
癌症研究
血管生成
眼科
血管内皮生长因子受体
内科学
免疫学
免疫系统
化疗
作者
Shiqi Yang,Tong Li,Huixun Jia,Min Gao,Yiming Li,Xiaoling Wan,Zhen Huang,Min Li,Yuanqi Zhai,Xiaomeng Li,Xiaotong Yang,Tao Wang,Jian Liang,Qing Gu,Xueting Luo,Lei Qian,Shujie Lu,Junjian Liu,Yanping Song,Fenghua Wang
标识
DOI:10.1126/scitranslmed.abj2177
摘要
Antiangiogenesis therapies targeting vascular endothelial growth factor (VEGF) have revolutionized the treatment of neovascular ocular diseases, including neovascular age-related macular degeneration (nAMD). Compelling evidence has implicated the vital role of complement system dysregulation in AMD pathogenesis, implying it as a potential therapeutic strategy for geographic atrophy in dry AMD and to enhance the efficacy of anti-VEGF monotherapies in nAMD. This study reports the preclinical assessment and phase 1 clinical outcomes of a bispecific fusion protein, efdamrofusp alfa (code: IBI302), which is capable of neutralizing both VEGF isoforms and C3b/C4b. Efdamrofusp alfa showed superior efficacy over anti-VEGF monotherapy in a mouse laser-induced choroidal neovascularization (CNV) model after intravitreal delivery. Dual inhibition of VEGF and the complement activation was found to further inhibit macrophage infiltration and M2 macrophage polarization. Intravitreal efdamrofusp alfa demonstrated favorable safety profiles and exhibited antiangiogenetic efficacy in a nonhuman primate laser-induced CNV model. A phase 1 dose-escalating clinical trial (NCT03814291) was thus conducted on the basis of the preclinical data. Preliminary results showed that efdamrofusp alfa was well tolerated in patients with nAMD. These data suggest that efdamrofusp alfa might be effective for treating nAMD and possibly other complement-related ocular conditions.
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