A Study of AAV9 Gene Therapy in Participants With Canavan Disease (CANaspire Clinical Trial)
Start Date
9/8/2021
Completion Date
10/8/2032
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.
Detailed Description
Canavan disease is an ultra-rare, profoundly disabling and fatal disease with no approved therapy. The Sponsor is developing BBP-812, an investigational gene therapy product for systemic delivery in participants with Canavan disease. BBP-812 is a recombinant adeno-associated virus serotype 9 (rAAV9) vector engineered to deliver the aspartoacylase (ASPA) transgene under control of a ubiquitous promoter to restore ASPA expression in both neuronal and non-neuronal cell types.
Eligibility Criteria
Age Range: No minimum to No maximum
Interventions
AAV9 BBP-812
Conditions
Locations
UCSF Benioff Children's Hospital Oakland
Oakland, California 94609
United States
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois 60611
United States
Massachusetts General Hospital (MGH); Center for Rare Neurological Diseases (CRND)
Boston, Massachusetts 02114
United States
Weill Cornell Medicine; Division of Pediatric Neurology
New York, New York 10065
United States