Clinical Research Directory
Browse clinical research sites, groups, and studies.
Evaluation of the Safety, Tolerability and Efficacy of a Gene Therapy Drug for the Treatment of Pediatric Fabry Disease
Sponsor: Children's Hospital of Fudan University
Summary
This is a single-arm, open label, single-dose clinical study to evaluate the safety, tolerability and efficacy of BBM-F101 injection in the pediatric Fabry disease participants up to 52 weeks after infusion, and the long-term safety and efficacy of BBM-F101 injection up to 5 years after infusion. BBM-F101 injection is an adeno-associated virus (AAV) gene therapy product for the treatment of pediatric Fabry disease.
Official title: A Single-arm, Open Label, Single-dose Clinical Study to Evaluate the Safety, Tolerability and Efficacy of BBM-F101 Injection in the Treatment of Pediatric Fabry Disease
Key Details
Gender
All
Age Range
7 Years - 18 Years
Study Type
INTERVENTIONAL
Enrollment
6
Start Date
2024-02-20
Completion Date
2029-06
Last Updated
2024-07-09
Healthy Volunteers
No
Conditions
Interventions
BBM-F101 injection
The dose of BBM-F101 injection will be calculated according to the participant's weight with single intravenous infusion.
Locations (1)
Children's Hospital of Fudan University
Shanghai, China