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Safety and Efficacy Study of Novel Gene Therapy AGX-08 for Geographic Atrophy

2026年7月30日 更新者:Zhongmou Therapeutics

Prospective, Dose-Escalating, Investigator Initiated Trial to Evaluate the Safety and Efficacy of AGX-08 in Geographic Atrophy

This is AGX-08's safety, tolerability, and efficacy in Geographic Atrophy first-in-human study. This trial is meant to evaluate the safety and efficacy of AGX-08 in Geographic Atrophy patients. Unilateral intravitreal injections (IVT) will be given into the subject's Study Eye.

研究概览

详细说明

Geographic atrophy (GA) secondary to age-related macular degeneration (AMD) is a leading cause of irreversible vision loss in the elderly population. Patients with GA experience progressive degeneration of retinal cells, resulting in gradual and permanent visual decline. Currently, there are limited effective treatment options available. We have developed an innovative adeno-associated virus (AAV)-based gene therapy for patients with GA, regardless of underlying genetic background. Approximately 8 to 24 subjects with GA will be recruited, among whom a subset will receive a single unilateral intravitreal injection of AGX-08 at ascending doses, while a proportion of subjects will receive sham injections as the control group.

研究类型

介入性

注册 (估计的)

24

阶段

  • 第一阶段早期

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

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Clinically confirmed diagnosis of geographic atrophy (GA) secondary to age-related macular degeneration (AMD);
  2. Age ≥ 50 years, regardless of sex;
  3. Best-corrected visual acuity (BCVA) in the study eye measured using the ETDRS chart at a starting distance of 4 meters must be ≤35 letters (Snellen equivalent ≤20/200), with vision no worse than light perception; the fellow eye must not have better visual acuity than the study eye;
  4. GA lesion size between 2.5 and 17.5 mm² with clearly defined borders. For multifocal GA, at least one lesion must be ≥1.25 mm² (0.5 disc area) to ensure measurable efficacy assessment;
  5. Presence of choroidal neovascularization (CNV) in the fellow eye is allowed;
  6. Women of childbearing potential must have a negative pregnancy test (blood or urine);
  7. Women of childbearing potential and male participants must agree to use effective contraception during the study and for 3 months after completion, with no plans for reproduction;
  8. Willing and able to provide written informed consent and comply fully with the study protocol.

Exclusion Criteria:

  1. GA caused by conditions other than AMD (e.g., Stargardt disease, cone-rod dystrophy, or other inherited macular dystrophies);
  2. Aphakia in the study eye, or cataract surgery/YAG capsulotomy within 3 months prior to screening;
  3. Refractive status or axial length outside the following range: spherical equivalent between -6.00D and +5.00D, and axial length between 21 mm and 26 mm;
  4. Two baseline BCVA measurements (ETDRS) taken at least 14 days apart during screening differ by >30%;
  5. Current or prior evidence of exudative (wet) AMD in the study eye, including retinal pigment epithelium tear, retinal vascular occlusions, history of corneal transplantation, or any neovascularization confirmed by fluorescein angiography;
  6. Active ocular diseases in the study eye, including inflammation, other macular diseases, glaucoma, ocular hypertension, or acute/chronic ocular infections;
  7. Major ocular surgery within 3 months prior to screening;
  8. History of retinal detachment or other fundus diseases unsuitable for study participation;
  9. Prior macular laser photocoagulation with irreversible retinal damage;
  10. Pregnant or lactating women, or participants unwilling to use effective contraception for 12 months before and after study intervention;
  11. Narrow anterior chamber angle or other contraindications to pupil dilation;
  12. Any ocular condition that may interfere with visual acuity assessment, OCT, or other ophthalmic evaluations;
  13. History of hypersensitivity to contrast agents, study drugs, or excipients;
  14. Allergy to corticosteroids, intolerance to protocol-required corticosteroid therapy, or contraindicated active infections;
  15. Severe systemic diseases, psychiatric disorders, uncontrolled chronic conditions, or other medical conditions that may increase study risk (e.g., malignancy, metabolic or autoimmune diseases);
  16. articipants with a prior history of malignancy must have completed curative treatment ≥5 years before enrollment and must have no evidence of active disease, recurrence, or metastasis. Participants whose prior malignancy is considered unlikely to affect life expectancy may be eligible based on Investigator assessment in consultation with an oncology specialist. The 5-year disease-free interval requirement may be waived for adequately treated cervical carcinoma in situ or non-melanoma skin cancer with minimal risk of recurrence.;
  17. Receiving or likely to receive immunosuppressive therapy outside this study;
  18. Participation in another investigational drug study within 3 months prior to screening;
  19. Prior gene therapy other than this study;
  20. Any condition that may compromise scientific evaluation of the study;
  21. Any contraindication to intravitreal (IVT) injection;
  22. Any other condition deemed unsuitable by the investigator.

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:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:Low Dose
IVT administration of a single low dose AGX-08 injection
rAAV2.AG-eNCRV intravitreal injection of low dose
其他名称:
  • 低剂量
实验性的:High Dose
IVT administration of a single high dose AGX-08 injection
rAAV2.AG-eNCRV intravitreal injection of high dose
其他名称:
  • 高剂量
假比较器:Control
Sham IVT injection
sham intravitreal injection of AGX-08 (not actual injection)
其他名称:
  • 假对照

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Incidence of treatment-emergent adverse events,adverse events, serious adverse events and dose-limiting toxicities
大体时间:baseline to Week 52
Incidence of severity of ocular and systemic treatment-emergent adverse events, (TEAEs), adverse events (AEs) , serious adverse events (SAEs) and dose-limiting toxicities(DLTs) following a single intravitreal injection of AGX-08.
baseline to Week 52

次要结果测量

结果测量
措施说明
大体时间
Change in Fundus Autofluorescence (FAF)
大体时间:baseline to Week 52
FAF is a non-invasive imaging technique that provides critical information about the health of the retina, which is vital for the functioning of the retina.
baseline to Week 52
Change in best corrected visual acuity (BCVA)
大体时间:baseline to Week 52
BCVA of both eyes will be assessed using the early treatment of diabetic retinopathy study (ETDRS) chart or tumbling "E" chart or other avaliable measurement. This approach was chosen to facilitate visual acuity testing in subject who cannot recognize letters.
baseline to Week 52

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7月1日

初级完成 (估计的)

2028年12月30日

研究完成 (估计的)

2029年12月30日

研究注册日期

首次提交

2026年5月17日

首先提交符合 QC 标准的

2026年5月20日

首次发布 (实际的)

2026年5月22日

研究记录更新

最后更新发布 (实际的)

2026年7月31日

上次提交的符合 QC 标准的更新

2026年7月30日

最后验证

2026年7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

不

研究美国 FDA 监管的设备产品

不

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