Search for Clinical Trial Results
Neuromyelitis Optica - 19 Studies Found
| Status | Study |
| Enrolling by invitation |
Study Name: Autologous Mesenchymal Stem Cells for the Treatment of Neuromyelitis Optica Spectrum Disorders Condition:
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| NOT_YET_RECRUITING |
Study Name: Observational Safety Study in Women With Neuromyelitis Optica Spectrum Disorder (NMOSD) Exposed to UPLIZNA� During Pregnancy Condition: Date: 2025-11-04 Interventions: Enrolled female participants with NMOSD who were exposed to UPLIZNA during pregnancy will be assessed.No study drug will be administered. |
| NOT_YET_RECRUITING |
Study Name: Inebilizumab in Acute Neuromyelitis Optica Spectrum Disorders Condition: Date: 2025-11-04 Interventions: Inebilizumab: 300mg IV on Day1 and Day 15.The first dose of inelizumab is given during IVMP. |
| Completed |
Study Name: Performance and Safety of a Digital Tool for Unsupervised Self-assessment of NMOSD Condition: Neuromyelitis Optica Date: 2025-11-04 Interventions: NMOSDCopilot includes active tests for walking, cognition, dexterity and vision, and e-questionnaires related to pain, fatigue, quality of life, bladd |
| Completed |
Study Name: Pediatric NMOSD Observational Study Condition: Neuromyelitis Optica Date: 2025-11-04 |
| Completed |
Study Name: In Vitro Study of the Biological and Immunological Activity of Imotopes� Candidates on Blood Cells of Patients With Stabilized NMO Condition: Neuromyelitis Optica Date: 2025-11-04 Interventions: The patients will be asked to provide at least 2 peripheral blood samples of approximately 100 milliliters each time, with a minimum of 14 days interv |
| COMPLETED |
Study Name: Efficacy and Safety of Mitoxantrone Hydrochloride Liposome Injection in the Treatment of Neuromyelitis Optica Spectrum Disorder (NMOSD) Condition: Neuromyelitis Optica Spectrum Disorder Date: 2025-11-04 Interventions: IV, once every 12 weeks (Q12W) |
| COMPLETED |
Study Name: BLAZE-Limiting Approach in NMOSD Condition: Neuromyelitis Optica Spectrum Disorders (NMOSD) Date: 2025-11-04 Interventions: Eculizumab was administered intravenously at a dosage of 900 mg weekly for four consecutive weeks |
| COMPLETED |
Study Name: Evaluate the Safety and Efficacy of CAR-T Cells in the Treatment of R/R Neuromyelitis Optica Condition: Neuromyelitis Optica Date: 2025-11-04 Interventions: CAR-T cells in the treatment of R/R neuromyelitis optica |