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Safety and Efficacy Study of PUMCH-E111 Injection in Subjects With RLBP1 Related Inherited Retinal Dystrophy

2026年6月15日 更新者:Peking Union Medical College Hospital

An Open-Label, Single-Center, Dose-Escalation Clinical Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of Intravitreal Injection of PUMCH-E111 in Subjects With RLBP1 Related Inherited Retinal Dystrophy

The goal of this clinical trial is to evaluate the safety and efficacy of PUMCH-E111 injection in subjects with RLBP1 related Inherited Retinal Dystrophy.

研究概览

详细说明

This is an open-label, single-center, dose-escalation study. One eye of each participant will receive a single intravitreal injection of PUMCH-E111. Participants will be followed for 52 weeks after which they will continue to be followed for up to 5 years after enrollment.

研究类型

介入性

注册 (估计的)

6

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

  • 姓名:Ruifang Sui, MD, PhD
  • 电话号码:+8613511017280
  • 邮箱:hrfsui@163.com

学习地点

    • Beijing Municipality
      • Beijing、Beijing Municipality、中国、100730
        • 招聘中
        • Peking Union Medical College Hospital
        • 接触:
          • Ruifang Sui, MD, PhD
          • 电话号码:+8613511017280
          • 邮箱:hrfsui@163.com
        • 首席研究员:
          • Ruifang Sui, MD, PhD

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

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Subjects voluntarily participate and sign the informed consent form;
  2. Age between 18-55 years old, gender is not limited;
  3. Clinical diagnosis of IRD caused by RLBP1 mutations;
  4. For the study eye, residual visual field within the 30° central field is tested using Program G or Program LVC on the Octopus perimeter;
  5. At screening, the blood pregnancy test result of females of childbearing potential (e.g., females who have not undergone surgical sterilization or less than 1 year after menopause) is negative. Male and female subjects of childbearing potential agree to use effective contraception throughout the study and for at least 12 months after dosing.

Exclusion Criteria:

  1. Opacity of refractive media or inability to dilate pupils in the study eye that significantly interferes with visual acuity detection, anterior segment or fundus assessment;
  2. Presence of diabetic retinopathy, retinal vein occlusion, pathological myopia, retinal detachment, or other conditions in the study eye that are assessed by the investigator as affecting the safety of the subject or the validity of the study;
  3. Active intraocular or periocular infection (such as blepharitis, conjunctivitis, keratitis, scleritis, etc.) in the study eye;
  4. History of vitreous hemorrhage in the study eye within 6 months prior to screening;
  5. Any intraocular surgery in the study eye within 3 months prior to screening;
  6. History of glaucoma in either eye;
  7. History of uveitis in either eye;
  8. Those with diffuse intravascular coagulation and obvious bleeding tendency (such as hemoptysis, hematemesis, severe purpura, etc.) within 3 months before screening;
  9. History of myocardial infarction, unstable angina, coronary revascularization, cerebrovascular accident (including TIA), history of other thromboembolic diseases (such as thromboembolic angiitis, pulmonary embolism, deep vein thrombosis, portal vein thrombosis, etc.), New York Heart Association (NYHA) grade ≥ II cardiac insufficiency, severe unstable ventricular arrhythmia, within 6 months prior to screening;
  10. Subjects with systemic immune diseases (including systemic lupus erythematosus, ankylosing spondylitis, rheumatoid arthritis, etc.);
  11. Diabetic patients with any of the following conditions: Known macrovascular complications or Glycosylated hemoglobin at screening(HbA1c)>7.5% or Those who have received more than two oral hypoglycemic drugs or received insulin or GLP-1 receptor agonists therapies;
  12. Hypertensive patients with poor blood pressure control (defined as: systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥100 mmHg when the subject is seated after receiving antihypertensive medication);
  13. Any uncontrollable clinical illness (such as severe psychiatric, respiratory and other systemic diseases and history of malignant tumors);
  14. Subjects with abnormal liver and kidney function: alanine aminotransferase (ALT)/aspartate aminotransferase (AST) ≥ 2 times the upper limit of normal; Total bilirubin ≥ 1.5 times the upper limit of normal, creatinine and urea/urea nitrogen ≥ 1.5 times the upper limit of normal;
  15. Subjects with abnormal coagulation function: prothrombin time (PT) > upper limit of normal value of 3 seconds or activated partial thromboplasting time (APTT) > upper limit of normal value of 10 seconds; Haemoglobin (HGb) < 10 g/dL;
  16. Those who are positive for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, treponema pallidum antibody and human immunodeficiency virus (HIV) antibody;
  17. Those who are known to be allergic to the therapeutic drugs or diagnostic drugs used in the study protocol, including the investigational products, etc.;
  18. Those who have used anticoagulant or antiplatelet drugs within 7 days before dosing;
  19. Currently using or may need to use drugs that can cause crystalline toxicity or retinal toxicity (such as deferoxamine, chloroquine/hydroxychloroquine, tamoxifen, ethambutol, etc.);
  20. Those who have a history of surgical operation within 1 month before screening, and/or currently have unhealed wounds (wound degree> stage III), moderate to severe ulcers, and fractures;
  21. Subjects with systemic infectious diseases requiring systemic treatment (oral, intramuscular or intravenous) at the time of screening;
  22. Those who have received any AAV gene therapy products in the past;
  23. Pregnant or lactating females;
  24. Those who have participated in any clinical trial of drugs (excluding vitamins and minerals) within 3 months before screening;
  25. Other individuals who need to be excluded, as determined 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: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:PUMCH-E111 Treatment Arm(Low dose)
Intraocular injection of a single low dose of PUMCH-E111
Single intravitreal injection
实验性的:PUMCH-E111 Treatment Arm(High dose)
Intraocular injection of a single high dose of PUMCH-E111
Single intravitreal injection

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
AE 发生率
大体时间:52周
总体和眼部不良事件 (AE) 的数量和严重程度
52周
严重不良事件的发生率
大体时间:52周
总体和眼部严重不良事件 (SAE) 的数量和严重程度
52周
DLT 的发生率
大体时间:4周
剂量限制毒性 (DLT) 的数量和比例
4周

次要结果测量

结果测量
措施说明
大体时间
视觉功能
大体时间:52周
BCVA(最佳矫正视力)(ETDRS)相对于基线的变化
52周
视觉功能
大体时间:52周
平均灵敏度 (MS) 相对于基线的变化(静态视野)
52周
Visual function
大体时间:52 weeks
Change from baseline in LLVA (Low-Luminance Visual Acuity) (ETDRS)
52 weeks
Visual function
大体时间:52 weeks
Change from baseline in the mean value of the photosensitivity threshold (Dark adaption Threshold Curve)
52 weeks

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。

调查人员

  • 首席研究员:Ruifang Sui, MD, PhD、Peking Union Medical College Hospital, Department of Ophthalmology

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 (实际的)

2026年2月3日

初级完成 (估计的)

2027年6月30日

研究完成 (估计的)

2031年5月31日

研究注册日期

首次提交

2026年6月15日

首先提交符合 QC 标准的

2026年6月15日

首次发布 (实际的)

2026年6月18日

研究记录更新

最后更新发布 (实际的)

2026年6月18日

上次提交的符合 QC 标准的更新

2026年6月15日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

其他研究编号

  • PUMCH-E111

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

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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