Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.
Drugs. 2021 Nov;81(17):2057-2062. doi: 10.1007/s40265-021-01623-w.
Vosoritide (VOXZOGO) is a modified recombinant human C-type natriuretic peptide (CNP) analogue, being developed by BioMarin Pharmaceutical for the treatment of achondroplasia. Achondroplasia is caused by a gain-of-function mutation in the fibroblast growth factor receptor 3 gene (FGFR3), which is a negative regulator of bone growth. Vosoritide acts to restore chondrogenesis through its binding to natriuretic peptide receptor B (NPR-B), resulting in the inhibition of downstream signalling pathways of the overactive FGFR3 gene. Vosoritide was approved in August 2021 in the EU for the treatment of achondroplasia in patients aged ≥ 2 years whose epiphyses are not closed; the diagnosis of achondroplasia should be confirmed by appropriate genetic testing. The drug is also under regulatory review in the USA for the treatment of achondroplasia and clinical development is underway in several countries. This article summarizes the milestones in the development of vosoritide leading to this first approval for achondroplasia in patients aged ≥ 2 years whose epiphyses are not closed.
Vosoritide(沃索利肽)是一种经过修饰的重组人 C 型利钠肽(CNP)类似物,由 BioMarin 制药公司开发,用于治疗软骨发育不全症。软骨发育不全症是由成纤维细胞生长因子受体 3 基因(FGFR3)的功能获得性突变引起的,该基因是骨骼生长的负调节剂。Vosoritide 通过与利钠肽受体 B(NPR-B)结合来恢复软骨生成,从而抑制过度活跃的 FGFR3 基因的下游信号通路。Vosoritide 于 2021 年 8 月在欧盟获得批准,用于治疗年龄≥2 岁且骺板未闭合的软骨发育不全症患者;软骨发育不全症的诊断应通过适当的基因检测确认。该药也正在美国接受监管审查,用于治疗软骨发育不全症,并且正在多个国家进行临床开发。本文总结了 vosoritide 的开发里程碑,最终该药在欧盟获得批准,用于治疗年龄≥2 岁且骺板未闭合的软骨发育不全症患者。