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Study of NBIB-223 Gene Therapy in Friedreich's Ataxia (FACET)

2026年11月6日 更新者:Neurocrine Biosciences

Phase 1/2, Open-Label, Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Efficacy of a Single Intravenous Infusion of NBIB-0000223 in Patients With Friedreich's Ataxia

This is a first-in-human study to evaluate the safety, tolerability, and pharmacodynamics of NBIB-0000223 (hereafter referred to as NBIB-223) in participants with Friedreich's Ataxia.

研究概览

地位

尚未招聘

研究类型

介入性

注册 (估计的)

24

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Neurocrine Medical Information Call Center
  • 电话号码:1-877-641-3461
  • 邮箱:medinfo@neurocrine.com

学习地点

    • California
      • Los Angeles、California、美国、90095
        • Neurocrine Clinical Site
    • Florida
      • Gainesville、Florida、美国、32608
        • Neurocrine Clinical Site
      • Tampa、Florida、美国、33612
        • Neurocrine Clinical Site
    • Iowa
      • Iowa City、Iowa、美国、52242
        • Neurocrine Clinical Site
    • Pennsylvania
      • Philadelphia、Pennsylvania、美国、19406
        • Neurocrine Clinical Site

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

8年 至 40年 (孩子、成人)

接受健康志愿者

不

有资格学习的性别

全部

描述

Key Inclusion Criteria:

  • Has both a clinical and genetic diagnosis of Friedreich's Ataxia, with diagnosis occurring at least 1 year prior to Screening and when the participant was age ≤16 years.

    • Documented prior genetic diagnosis of Friedreich's Ataxia with a pathogenic GAA trinucleotide repeat expansion in intron 1 of both frataxin alleles, based on analysis by a Clinical Laboratory Improvement Amendments (CLIA)-certified laboratory.
    • Clinical evidence of symptomatic neurologic disease consistent with Friedreich's Ataxia.
    • Have an Modified Friedreich Ataxia Rating Scale (mFARS) overall score ≥15 and <80, and an Modified Friedreich Ataxia Rating Scale subscale E: Upright Stability (mFARS-E) gait score of ≥1.
  • Participants who are currently taking omaveloxolone must have initiated treatment at least 1 year prior to Screening and have been on a stable dose for at least 12 weeks prior to Screening, with no anticipated dose adjustments during the 48-week period following NBIB-223 infusion.

  • Participants who are not currently taking omaveloxolone must agree not to start taking omaveloxolone during the 48-week period following NBIB-223 infusion.

Key Exclusion Criteria:

  • Pregnant, plan to become pregnant during the first 12 months of the study, or lactating.
  • Have protocol-specified laboratory abnormalities at screening.
  • Previous exposure to adeno-associated virus (AAV)-9 as determined by the presence of serum total anti-AAV9 antibodies (TAb).
  • Contraindication to cerebrospinal fluid collection via lumbar puncture, magnetic resonance imaging with contrast, or endomyocardial biopsy.
  • Have had a myocardial infarction, cerebrovascular accident, thromboembolic event, or transient ischemic attacks, or have evidence of myocardial ischemia and/or clinically significant cardiac valve disease, obstructive cardiac disease, or arrhythmias.
  • Have an ongoing medical condition that, in the opinion of the investigator, would compromise the participant's safety or successful participation in the study or interpretation of study results.
  • Have uncontrolled diabetes (hemoglobin [Hb] A1c >8.0%)
  • Have an active fungal, bacterial, or viral infection.
  • Have scheduled or planning to schedule surgical treatment for scoliosis, foot deformity, or other indications during the first 18 months of the study that will interfere with the participant's ability to complete study assessments.
  • Any history of participation in a cellular or gene therapy clinical study, or any history of having been treated with a cellular or gene therapy.
  • Have participated in any other interventional clinical study within 30 days prior to Study Day 1 or receipt of any investigational product within the 30 days of enrollment or 5 half-lives of the investigational product, whichever is longer.

Additional inclusion/exclusion criteria may apply, per protocol.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:非随机化
  • 介入模型:顺序分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Part A: NBIB-223

Dose escalation in adult participants.

Intravenous (IV) infusion

其他名称:
  • NBIB-223
实验性的:Part B: NBIB-223

Dose expansion in pediatric participants.

Intravenous (IV) infusion

其他名称:
  • NBIB-223
实验性的:Part C: NBIB-223

Dose expansion in adult and/or pediatric participants with FA-related cardiomyopathy.

Intravenous (IV) infusion

其他名称:
  • NBIB-223

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Number of Participants with Treatment-emergent Adverse Events
大体时间:Day 1 through 48-Week Post-Treatment Follow-Up
Day 1 through 48-Week Post-Treatment Follow-Up

次要结果测量

结果测量
大体时间
Change from Baseline in Frataxin Protein Expression
大体时间:Baseline, up to 48-Week Post-Treatment Follow-Up
Baseline, up to 48-Week Post-Treatment Follow-Up

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2028年11月1日

研究完成 (估计的)

2032年11月1日

研究注册日期

首次提交

2026年11月6日

首先提交符合 QC 标准的

2026年11月6日

首次发布 (实际的)

2026年11月12日

研究记录更新

最后更新发布 (实际的)

2026年11月12日

上次提交的符合 QC 标准的更新

2026年11月6日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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