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A Study of AAV9 Gene Therapy in Participants With Canavan Disease (CANaspire Clinical Trial)
Sponsor: Aspa Therapeutics
Summary
The main objective of this trial is to evaluate the safety, tolerability, and pharmacodynamic activity of BBP-812, an investigational AAV9-based gene therapy, in pediatric participants with Canavan disease.
Official title: A Phase 1/2 Open-Label Study of the Safety and Clinical Activity of Gene Therapy for Canavan Disease Through Administration of an Adeno-Associated Virus (AAV) Serotype 9-Based Recombinant Vector Encoding the Human ASPA Gene
Key Details
Gender
All
Age Range
Any - 30 Months
Study Type
INTERVENTIONAL
Enrollment
26
Start Date
2021-09-08
Completion Date
2030-10-08
Last Updated
2024-10-22
Healthy Volunteers
No
Conditions
Interventions
AAV9 BBP-812
Sterile solution for injection for 1-time use via volumetric infusion pump
Locations (4)
UCSF Benioff Children's Hospital Oakland
Oakland, California, United States
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois, United States
Massachusetts General Hospital (MGH); Center for Rare Neurological Diseases (CRND)
Boston, Massachusetts, United States
Weill Cornell Medicine; Division of Pediatric Neurology
New York, New York, United States