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NOT YET RECRUITING
NCT06561009
PHASE1/PHASE2
Safety and Efficacy of BAFFR CART for Relapsed/ Refractory Neuromyelitis Optica Spectrum Disorder
Sponsor: Tianjin Medical University General Hospital
View on ClinicalTrials.gov
Summary
This is an open-label, single-arm, dose-escalation study in up to 20 participants with relapsed/refractory Neuromyelitis Optica Spectrum Disorders (NMOSD). The aim is to evaluate the safety and efficacy of the treatment with BAFFR CART.
Key Details
Gender
All
Age Range
18 Years - 60 Years
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2025-12-01
Completion Date
2028-10-01
Last Updated
2025-05-30
Healthy Volunteers
No
Conditions
Interventions
DRUG
Anti-BAFFR CART
Anti-BAFFR CART