首页> 美国卫生研究院文献>Orphanet Journal of Rare Diseases >Lucerastat an iminosugar with potential as substrate reduction therapy for glycolipid storage disorders: safety tolerability and pharmacokinetics in healthy subjects
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Lucerastat an iminosugar with potential as substrate reduction therapy for glycolipid storage disorders: safety tolerability and pharmacokinetics in healthy subjects

机译:Lucerastat一种亚氨基糖可能作为糖脂贮积症的底物减少疗法:健康受试者的安全性耐受性和药代动力学

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摘要

BackgroundLucerastat, an inhibitor of glucosylceramide synthase, has the potential to restore the balance between synthesis and degradation of glycosphingolipids in glycolipid storage disorders such as Gaucher disease and Fabry disease. The safety, tolerability, and pharmacokinetics of oral lucerastat were evaluated in two separate randomized, double-blind, placebo-controlled, single- and multiple-ascending dose studies (SAD and MAD, respectively) in healthy male subjects.
机译:背景技术葡糖胺神经酰胺合酶的抑制剂Lucerastat有潜力恢复糖脂储存疾病(例如高雪氏病和法布里氏病)中糖鞘脂的合成和降解之间的平衡。在健康男性受试者的两项独立,随机,双盲,安慰剂对照,单次和多次递增剂量研究(分别为SAD和MAD)中评估了口服lucerastat的安全性,耐受性和药代动力学。

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