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Eculizumab For Acute Attack of Neuromyelitis Optica Spectrum Disorder (NMOSD): a Multi-Center, Phase 2 Trial (EASE-NMO)
Neuromyelitis optica spectrum disorder (NMOSD) is a relapsing, inflammatory autoimmune disorder of the central nervous system characterized by the pathogenic anti-aquaporin 4 antibody (AQP4-IgG). The objectives of this study are to assess the efficacy and safety of eculizumab for treatment of patients with neuromyelitis optica spectrum disorders during acute phase who are anti-aquaporin-4 (AQP4) antibody-positive. Eculizumab, a humanized monoclonal antibody, inhibits the terminal complement protein C5 and prevents its cleavage into C5a and the formation of C5b-9 (MAC), has approved for preventive treatment of NMOSD. Given the high efficacy of C5 inhibition, eculizumab is proposed to potentially provide rapid relief from astrocyte destruction by reducing MAC formation, which could contribute to the fast alleviation of neurological deficit during NMO acute attack. The potential of eculizumab warrants further investigation as a treatment for acute neuromyelitis optica spectrum disorders attacks.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Tianjin Medical University General Hospital
Tianjin, Tianjin Municipality, China
Start Date
September 9, 2025
Primary Completion Date
August 31, 2026
Completion Date
December 31, 2026
Last Updated
September 22, 2025
110
ESTIMATED participants
Intravenous Methylprednisolone (IVMP)
DRUG
Complement protein C5 inhibitor
DRUG
Lead Sponsor
Tianjin Medical University General Hospital
Data Source & Attribution
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