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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

Interventions

DRUG

Anti-BAFFR CART

Anti-BAFFR CART