Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06561009

Safety and Efficacy of BAFFR CART for Relapsed/ Refractory Neuromyelitis Optica Spectrum Disorder

Status
Not Yet Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Tianjin Medical University General Hospital · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGAnti-BAFFR CARTAnti-BAFFR CART

Timeline

Start date
2025-12-01
Primary completion
2027-10-01
Completion
2028-10-01
First posted
2024-08-19
Last updated
2025-05-30

Source: ClinicalTrials.gov record NCT06561009. Inclusion in this directory is not an endorsement.