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A Phase I/II Clinical Study to Evaluate the Safety and Efficacy of VGN-R08b in Patients With Type III Gaucher's Disease

2026年5月20日 更新者:Shanghai Vitalgen BioPharma Co., Ltd.

A Phase I/II Clinical Study to Evaluate the Tolerance, Safety and Efficacy of VGN-R08b Intracerebroventricular Injection in Patients With Type III Gaucher's Disease

A phase I/II clinical study to evaluate the tolerance, safety and efficacy of VGN-R08b intracerebroventricular injection in patients with type III Gaucher's disease

研究概览

详细说明

This is an open-label, dose-escalation clinical trial, consisting of dose escalation and dose expansion. A total of 12 subjects are expected to be enrolled.

Dose escalation: Initially, three doses of 6×10^10 vg/g, 1.2×10^11 vg/g, and 1.8×10^11 vg/g (per unit brain weight) are planned to be explored . Three subjects will be enrolled in each dose group. The second and third subjects in the same dose group must be confirmed to be safe and tolerable after at least a 4-week safety assessment of the first subject before receiving the drug. For the high-dose group (1.8×10^11 vg/g), subjects will be enrolled one by one.

Dose expansion: After the dose escalation is completed, the SRC will comprehensively evaluate the data on efficacy, safety, and immunogenicity, etc., to select the optimal effective dose and expand the enrollment by 3 cases.

研究类型

介入性

注册 (估计的)

12

阶段

  • 阶段2
  • 阶段1

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

  • 孩子
  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  1. The signing of the informed consent form should be completed when the subject is at least 2 years old but less than 18 years old.
  2. The subject has a documented medical history of Gaucher disease confirmed by GCase enzyme activity testing, and has a double GBA1 gene mutation.
  3. According to the investigator's assessment, the neurological signs and/or symptoms are consistent with type III Gaucher disease.
  4. At the time of enrollment, the subject has horizontal eye movement disorders (including gaze paralysis, or delayed or absent saccades), but there is no severe motor dysfunction resulting in bedridden status.
  5. The subject is currently receiving substrate reduction therapy (SRT) and/or high-dose ambroxol for Gaucher disease treatment. The subject is required to have been on stable treatment for at least 2 months before enrollment and the investigator determines that the treatment is ineffective for neurological symptoms, or is willing to discontinue the treatment at the time of enrollment (discontinuation 1 week before administration).
  6. The subject is currently receiving and willing to continue stable peripheral treatment (including imiglucerase or other ERT, or SRT), and the peripheral symptoms of Gaucher disease are stable at the time of screening, that is, all of the following conditions are met: hemoglobin level ≥ 11.0 g/dL (female) or ≥ 12.0 g/dL (male), platelet count ≥ 100×109/L, spleen volume < 10 times the normal value (MN), liver volume < 1.5 MN, and no bone crisis or asymptomatic bone disease (such as bone necrosis and/or pathological fractures causing bone pain) within 3 months before screening.
  7. (Applicable) Male and female subjects with reproductive potential must continue to use an effective contraceptive method (including abstinence) correctly from the screening period until at least 1 year after the start of treatment, and not donate sperm or eggs.
  8. The subject (applicable) and their parents/guardians must understand the trial information, purpose and risks described in the informed consent form, and authorize the use of the subject's health information and provide an informed consent form with the signature and date of signing.
  9. The subject (applicable) and their parents/guardians are willing to participate in the study as information providers, providing the subject's health status, cognition and physical ability (including providing information for rating scales).

Exclusion Criteria:

  1. There are other serious neurological disorders that may cause symptoms of Gaucher disease or interfere with the research objectives;
  2. There are severe internal organ damages caused by Gaucher disease, which, after evaluation by the researchers, are considered to pose unacceptable risks to the subjects, or interfere with the subjects' research compliance, or interfere with the execution of the trial;
  3. Long-term ventilation or long-term nasogastric feeding (long-term ventilation is defined as: requiring tracheotomy for respiratory assistance, or continuous 14 days or more of non-invasive respiratory assistance for ≥ 16 hours per day, excluding acute reversible diseases that require assisted ventilation and perioperative ventilation. Long-term nasogastric feeding refers to the use of a nasogastric tube for feeding due to severe loss of swallowing function);
  4. There are severe immunodeficiencies or autoimmune diseases;
  5. There is active infection (including viral infections such as HIV, HBV, HCV or syphilis);

    The following medication and treatment situations exist:

  6. Currently using drugs, herbs, or over-the-counter medications that have strong inhibitory or inducing effects on CYP3A4 or P-gp;
  7. Having received bone marrow or organ transplantation, or any gene or cell therapy;
  8. Having undergone immunization (live vaccines) within 4 weeks;
  9. Undergoing systemic immunosuppressive therapy or corticosteroid therapy other than that required by the protocol (local preparations for skin diseases can be used);

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:单组作业
  • 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:Dose group (1)
3 subjects on 6×10^10 vg/g for at least 4 weeks post injection
6×10^10 vg/g
1.2×10^11 vg/g
1.8×10^11 vg/g
实验性的:Dose group (2)
3 subjects on 1.2×10^11 vg/g for at least 4 weeks post injection
6×10^10 vg/g
1.2×10^11 vg/g
1.8×10^11 vg/g
实验性的:Dose group (3)
3 subjects on 1.8×10^11 vg/g for at least 4 weeks post injection
6×10^10 vg/g
1.2×10^11 vg/g
1.8×10^11 vg/g

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
Number of adverse events (AE), Serious adverse events (SAE)
大体时间:Up to 5 years
Vital signs, physical examination, laboratory test results will be monitored after drug injection
Up to 5 years

次要结果测量

结果测量
措施说明
大体时间
Changes in Glucose Gangliosidase (GCase)
大体时间:Up to 5 years
Changes in the activities of glucose gangliosidase (GCase) in peripheral blood and cerebrospinal fluid (CSF) after medication administration
Up to 5 years
Changes in Glucose sialic acid (Lyso-GL1)
大体时间:Up to 5 years
Changes in the levels of glucose sialic acid (Lyso-GL1) in peripheral blood and cerebrospinal fluid (CSF) after medication administration
Up to 5 years
Changes in electrooculogram
大体时间:Up to 5 years
Changes in pupillary reflex, horizontal eye movement and vertical eye movement after medication administration compared to the baseline
Up to 5 years
Changes in Scale for the Assessment and Rating of Ataxia
大体时间:Up to 5 years
Changes in ataxia, and the proportion of subjects whose ataxia symptoms showed significant improvement compared to the baseline
Up to 5 years
Viral shedding
大体时间:Up to 5 years
Changes in the genomic levels of the VGN-R08b vector in peripheral blood, urine, feces, and nasal mucosal secretions after medication administration
Up to 5 years
Immunogenicity
大体时间:Up to 5 years
The number of subjects who produced antibodies against AAV9 and GCase, as well as the antibody titers, including in serum and CSF
Up to 5 years

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5月14日

初级完成 (估计的)

2028年5月29日

研究完成 (估计的)

2032年8月16日

研究注册日期

首次提交

2026年4月30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5月22日

上次提交的符合 QC 标准的更新

2026年5月20日

最后验证

2026年5月1日

更多信息

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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