Yuen Yi Hon1, Jie Wang2, Henrietta Abodakpi2

  • 1Division of Rare Diseases and Medical Genetics, Office of Rare Diseases, Pediatrics, Urologic and Reproductive Medicine, Office of New Drugs (OND), Center of Drug Evaluation and Research (CDER), Food and Drug Administration (FDA), Silver Spring, Maryland, USA.

PubMed
概括

在先天性代谢错误 (IEM) 中,酶替代疗法 (ERT) 的有效剂量发现需要早期的体外和动物研究,然后进行强大的临床试验. 关键策略包括定义特定的终点和利用药理动力学生物标志物以获得最佳剂量.

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