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RECRUITING
NCT04998396
PHASE1/PHASE2

A Study of AAV9 Gene Therapy in Participants With Canavan Disease (CANaspire Clinical Trial)

Sponsor: Aspa Therapeutics

View on ClinicalTrials.gov

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

BIOLOGICAL

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