GALILEO-1: FLT201基因治疗1型戈谢病的I/II期安全性和有效性研究

D. Hughes, F. Ferrante
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引用次数: 0

摘要

戈谢病1型(GD1)由GBA1基因突变引起,导致β-葡萄糖脑苷酶(GCase)缺乏。基因治疗作为GD1患者的潜在治疗选择正在研究中。实验性基因疗法FLT201由一种腺相关病毒(AAVS3)编码一种新的GCase变体(GCase-85)组成。FLT201的临床前表征显示出令人乐观的结果,GCase-85在生理pH下比野生型GCase更稳定,并能有效地递送到靶组织。在这里,我们描述了GALILEO-1的设计,这是一项FLT201基因治疗成人GD1患者的首次人体I/II期安全性、耐受性和有效性研究。该研究结果将决定启动FLT201在GD1患者中的III期研究。临床试验注册:NCT05324943 (ClinicalTrials.gov)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GALILEO-1: a Phase I/II safety and efficacy study of FLT201 gene therapy for Gaucher disease type 1
Gaucher disease type 1 (GD1), caused by mutations in the GBA1 gene, results in β-glucocerebrosidase (GCase) deficiency. Gene therapy is under investigation as a potential treatment option for patients with GD1. The investigational gene therapy FLT201 consists of an adeno-associated virus (AAVS3) encoding a novel GCase variant (GCase-85). Preclinical characterization of FLT201 showed promising results, with GCase-85 being more stable at physiological pH than wild-type GCase and delivered effectively to target tissues. Here, we describe the design of GALILEO-1, a first-in-human Phase I/II safety, tolerability and efficacy study of FLT201 gene therapy in adult patients with GD1. The study results will inform the decision to start a Phase III study of FLT201 in patients with GD1. Clinical Trial Registration: NCT05324943 ( ClinicalTrials.gov )
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