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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

20. Mai 2026 aktualisiert von: 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

Studienübersicht

Status

Noch keine Rekrutierung

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

12

Phase

  • Phase 2
  • Phase 1

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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);

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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
Experimental: 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
Experimental: 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

Was misst die Studie?

Primäre Ergebnismessungen

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

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Changes in Glucose Gangliosidase (GCase)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

14. Mai 2026

Primärer Abschluss (Geschätzt)

29. Mai 2028

Studienabschluss (Geschätzt)

16. August 2032

Studienanmeldedaten

Zuerst eingereicht

30. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

20. Mai 2026

Zuerst gepostet (Tatsächlich)

22. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

22. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

20. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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