跳至主要内容
临床试验/NCT07095686
NCT07095686Enrolling By Invitation1 期

An Open-Label Study of an Experimental Antisense Oligonucleotide Treatment for Amyotrophic Lateral Sclerosis (ALS) Due to an Arg15Leu Pathogenic Variant in CHCHD10

n-Lorem Foundation2 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2024年10月2日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
Enrolling By Invitation
入组人数
9
试验地点
2
主要终点
Clinical Functioning

研究概览

简要总结

This research project entails delivery of a personalized antisense oligonucleotide (ASO) drug designed for individual participants with amyotrophic lateral sclerosis (ALS) due to a pathogenic variant in CHCHD10

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Informed consent/assent provided by the participant (when appropriate), and/or participant's parent(s) or legally authorized representatives(s)
  • Ability to travel to the study site and adhere to study related follow-up examinations and/or procedures and provide access to participant's medical records
  • Genetically confirmed neurological disorder

排除标准

  • Participant has any condition that in the opinion of the Site Investigator would ultimately prevent the completion of study procedures
  • Use of an investigational medication within less than 5 half-lives of the drug at enrollment

研究组 & 干预措施

Open Label nL-CHCHD-001

Experimental

干预措施: nL-CHCHD-001 (Drug)

结局指标

主要结局

Clinical Functioning

时间窗: Baseline to 12 months

Change from baseline at 12-months post nL-CHCHD-001 administration in scores on Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R).

Motor Function

时间窗: Baseline to 12 months

Change from baseline at 12-months post nL-CHCHD-001 administration in Slow Vital Capacity (SVC)

次要结局

  • Disease Biomarkers(Baseline to 12 months)
  • Safety and Tolerability(Baseline to 12 months)
  • Safety and tolerability(Baseline to 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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