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rAAV-Olig001-ASPA Gene Therapy for Treatment of Children With Typical Canavan Disease

Study acronym: CAN-GT
StatusEnrolling by Invitation
PhasePhase 1/2
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated November 14, 2025 (before its estimated August 31, 2026 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Minor Trial status: Recruiting to Enrolling by Invitation
    • Site details revised
    v12
  2. Minor Site contact updatedv11
  3. Notable Trial status: Active, Not Recruiting to Recruiting
    • Site details revised
    v10
  4. Minor Trial status: Enrolling by Invitation to Active, Not Recruitingv9
  5. Notable Trial status: Active, Not Recruiting to Enrolling by Invitation
    • Primary completion date: Aug 31, 2023 to Aug 31, 2026
    • Study completion date: Aug 31, 2024 to Aug 31, 2027
    v8
Show 6 earlier versionsHide 6 earlier versions
  1. Minor Trial status: Enrolling by Invitation to Active, Not Recruiting
    • Primary completion date: Mar 31, 2023 to Aug 31, 2023
    • Study completion date: Mar 31, 2024 to Aug 31, 2024
    v7
  2. Minor Trial status: Recruiting to Enrolling by Invitation
    • Site details revised
    v6
  3. Minor Interventions: Levetiracetam (Drug), Prednisolone (Drug), rAAV-Olig001-ASPA (Drug) to Levetiracetam (Drug), Prednisone (Drug), rAAV-Olig001-ASPA (Drug)
    • Secondary endpoints: 8 to 7
    • Eligibility criteria expanded, about 3 words
    v5
  4. Minor Re-verified, no change to tracked fieldsv4
  5. Notable Lead sponsor: CureRareDisease LLC to Myrtelle Inc.v3
  6. Minor Secondary endpoints: details revised at 3 of 8 entriesv2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Canavan Disease is a congenital white matter disorder caused by mutations to the gene encoding for aspartoacylase (ASPA). Expression of ASPA is restricted to oligodendrocytes, the sole white matter producing lineage in the brain. ASPA supports myelination in the capacity of its sole known function, namely, the catabolism of N-acetylaspartate (NAA). Inherited mutations that result in loss of ASPA catabolic activity result in a typically severe phenotype of Canavan Disease, characterized by chronically elevated brain NAA, gross motor abnormalities, hypomyelination, progressive spongiform degeneration of the brain, epilepsy, blindness, and a short life expectancy. Disease severity is correlated with residual levels of enzyme activity. Reconstitution of ASPA function in oligodendrocytes of the brains of Canavan patients is expected to rescue NAA metabolism in its natural cellular compartment and support myelination/remyelination by resident white matter producing cells. This protocol directly targets oligodendrocytes in the brain, which are intimately involved with disease initiation and progression. Targeting oligodendrocytes offers the safest and most direct therapy for affected individuals. The latest generation AAV viral vector (rAAV-Olig001-ASPA) will be administered to patients using neurosurgical procedure which involves direct administration of gene therapy to affected regions of the brain. Outcome measures for the open label clinical trial include longitudinal clinical assessments and brain imaging. Currently, there is no effective treatment for Canavan Disease. The purpose of this study is to validate a new technology targeted to the cells most affected by Canavan Disease in the safest way possible. The study investigators are committed to supporting the Rare Disease \& Canavan Disease Communities. For more information, please contact Jordana Holovach, Head of Communications and Community at PatientAdvocacy@myrtellegtx.com.
Trial Details
NCT Number NCT04833907
Lead Sponsor Myrtelle Inc.
Conditions
(from sponsor)
Canavan Disease
Related terms Canavan Disease
Enrollment 24 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov