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临床试验/NCT06565572
NCT06565572Enrolling By Invitation早期 1 期

An Open-label Single Center, Single Participant Study of an Experimental Antisense Oligonucleotide Treatment for PCARP (Posterior Column Ataxia With Retinitis Pigmentosa) Disease Due to Mutations in FLVCR1

University of Colorado, Denver2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2023年8月23日最近更新:
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
Enrolling By Invitation
入组人数
1
试验地点
2
主要终点
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

研究概览

简要总结

The goal of this clinical trial is to evaluate a specific antisense oligonucleotide medication in one patient with posterior column ataxia with retinitis pigmentosa. The main question it aims to answer is: what is the safety and tolerability of this medication in a single participant.

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

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 representative(s).
  • Genetically confirmed FLVCR1-related disease.
  • 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.

排除标准

  • Allergy to any of the ASO components
  • Participant has any condition that in the opinion of the Site Investigator, would ultimately prevent the completion of study procedures.

研究组 & 干预措施

nL-FLVC-001 Arm

Experimental

nL-FLVC-001 is an antisense oligonucleotide that will be injected into the vitreous

干预措施: nL-FLVC-001 (Drug)

结局指标

主要结局

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0

时间窗: Over 12 months

We will measure visual acuity, retinal thickness, examine changes in fundus photos and biomicroscopic exam post nL-FLVC-001 administration in a participant with FLVCR1 gene mutation

时间窗: Over 12 months

次要结局

  • Measure any changes in the Cardiff Visual Ability Questionnaire for Children (CVAQC-25) in one patient with PCARP after nL-FLVC-001 intravitreal injection.(Over 12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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