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临床试验/NCT07161544
NCT07161544招募中1 期

An Open-label, Multicenter, Two Part, Ascending Dose Followed by a Controlled Trial to Assess the Safety and Efficacy of a Subretinal Administration of AAVB-039 in Participants With Stargardt Disease (STGD1) (CELESTE)

AAVantgarde Bio Srl12 个研究点 分布在 2 个国家目标入组 75 人开始时间: 2025年9月29日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
75
试验地点
12
主要终点
To measure the number and severity of treatment related adverse events following treatment with AAVB-039

研究概览

简要总结

The purpose of the 039-101 study is to evaluate the safety and tolerability of a single subretinal injection of AAVB-039 in participants with Stargardt disease secondary to a biallelic mutation of the ABCA4 gene. The study will also assess initial efficacy following AAVB-039 administration.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
8 Years 至 55 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Molecular diagnosis of Stargardt disease due to ABCA4 mutation
  • Willingness to adhere to protocol per informed consent

排除标准

  • Unwillingness to meet the requirements of the study
  • Participation in a clinical study with another Investigation Medicinal Product
  • Previous participation in another gene or cell therapy trial
  • Any condition that would preclude subretinal surgery
  • Complicating ocular and/or systemic diseases

研究组 & 干预措施

Cohort 3

Experimental

AAVB-039 dose level 3 (high dose)

干预措施: AAVB-039 (Biological)

Cohort 1

Experimental

AAVB-039 dose level 1 (low dose)

干预措施: AAVB-039 (Biological)

Cohort 2

Experimental

AAVB-039 dose level 2 (mid dose)

干预措施: AAVB-039 (Biological)

Cohorts 4-5

Experimental

AAVB-039 dose level 1, 2 or 3

干预措施: AAVB-039 (Biological)

结局指标

主要结局

To measure the number and severity of treatment related adverse events following treatment with AAVB-039

时间窗: 0-60 months

次要结局

  • Change in ellipsoid zone (EZ) loss following treatment with AAVB-039(0-60 months)
  • Change in the area of atrophy (assessed via short wavelength fundus autofluorescence (SW-FAF), following treatment with AAVB-039(0-60 months)
  • Change in macular sensitivity assessed via microperimetry following treatment with AAVB-039(0-60 months)
  • Change in visual acuity following treatment with AAVB-039(0-60 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (12)

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