Keam Susan J
Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.
Drugs. 2023 Jun;83(9):819-824. doi: 10.1007/s40265-023-01883-8.
Trofinetide (DAYBUE™), an oral, small molecule, synthetic analog of glycine-proline-glutamate [GPE; the N-terminal tripeptide derivative of insulin like growth factor-1 (IGF-1)], is being developed by Neuren Pharmaceuticals and Acadia Pharmaceuticals for the treatment of rare childhood neurodevelopmental disorders. Trofinetide was approved in March 2023 in the USA for the treatment of Rett syndrome in adult and pediatric patients 2 years of age and older. This article summarizes the milestones in the development of trofinetide leading to this first approval for Rett syndrome.
曲非奈肽(DAYBUE™)是甘氨酸-脯氨酸-谷氨酸[GPE;胰岛素样生长因子-1(IGF-1)的N端三肽衍生物]的口服小分子合成类似物,目前正在由纽伦制药公司和阿卡迪亚制药公司开发,用于治疗罕见的儿童神经发育障碍。曲非奈肽于2023年3月在美国获批,用于治疗2岁及以上成人和儿童患者的雷特综合征。本文总结了曲非奈肽在开发过程中取得的里程碑式进展,最终实现了雷特综合征的首次获批。