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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

調査の概要

状態

まだ募集していません

詳細な説明

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.

研究の種類

介入

入学 (推定)

12

段階

  • フェーズ2
  • フェーズ 1

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人

健康ボランティアの受け入れ

いいえ

説明

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);

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:非ランダム化
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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
実験的: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
実験的: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

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Number of adverse events (AE), Serious adverse events (SAE)
時間枠:Up to 5 years
Vital signs, physical examination, laboratory test results will be monitored after drug injection
Up to 5 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Changes in Glucose Gangliosidase (GCase)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年5月14日

一次修了 (推定)

2028年5月29日

研究の完了 (推定)

2032年8月16日

試験登録日

最初に提出

2026年4月30日

QC基準を満たした最初の提出物

2026年5月20日

最初の投稿 (実際)

2026年5月22日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月22日

QC基準を満たした最後の更新が送信されました

2026年5月20日

最終確認日

2026年5月1日

詳しくは

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