Last updated: February 21, 2024
Sponsor: Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Overall Status: Active - Recruiting
Phase
1
Condition
Gaucher Disease
Treatment
VGN-R08b
Clinical Study ID
NCT06272149
VGN-R08b-001
Ages < 24 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Infants with age of ≤24 months.
- Historical diagnosis of Gaucher disease confirmed by GCase enzyme activity test, andwith GBA1 biallelic mutations.
- Neurological signs and/or symptoms consistent with diagnosis of GD2.
- Parent(s)/legal guardian(s) of subject must give their consent for subject to enrollin the study.
- Parent(s)/legal guardian(s) of the subject must agree to comply with the requirementsof the study, including providing disease information and support disease assessmentof symptoms.
Exclusion
Exclusion Criteria:
- Diagnosis of a significant CNS disease other than GD2 that may be a cause for thepatient's GD symptoms or may confound study objectives.
- Achieved independent gait.
- Severe visceral symptoms of GD which, in the opinion of the Investigator, would posean unacceptable risk to the patient or interfere with the patient's ability to complywith study procedures or interfere with the conduct of the study.
- Clinically active infection (including HIV, HBV, HCV or syphilis).
- For those receiving enzyme replacement therapy and/or substrate reduction therapyand/or ambroxol for Gaucher disease, stable treatment ≤2 months before enrollment.
- Use of strong inhibitors or inducers of cytochrome CYP3A4 or P-glycoprotein (P-gp)medications, herbals, or over-the-counter agents.
- Any type of prior gene or cell therapy.
- Immunizations (live vaccines) in the prior 4 weeks.
- Use of systemic immunosuppressant or corticosteroid therapy other thanprotocol-specified (topical preparations for dermatological conditions are allowed).
- Patients with anti-AAV9 neutralizing antibody titer over 1:5.
- Brain MRI (magnetic resonance imaging) showing clinically significant abnormalityconsidered to prevent intracisternal injection.
- Contraindication to sedation during surgery or imaging studies (PET).
- Presence of other significant medical conditions that would create an unacceptablerisk to the patient or interfere with the patient's ability to comply with studyprocedures or interfere with the conduct of the study.
Study Design
Total Participants: 6
Treatment Group(s): 1
Primary Treatment: VGN-R08b
Phase: 1
Study Start date:
March 01, 2023
Estimated Completion Date:
February 28, 2029
Study Description
Connect with a study center
Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai 200097
ChinaActive - Recruiting
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