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A real-world study of satralizumab in the treatment of neuromyelitis optica spectrum disorder (NMOSD)

A real-world study of satralizumab in the treatment of neuromyelitis optica spectrum disorder (NMOSD)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500109805
Enrollment
Unknown
Registered
2025-09-25
Start date
2025-10-01
Completion date
Unknown
Last updated
2025-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

neuromyelitis optica spectrum disorder, NMOSD

Interventions

Observation group:None

Sponsors

Xi'an No.1 Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosed with AQP-4 antibody positive NMOSD (meeting the diagnostic criteria of the 2015 International Neuro-Ophtalmology Society); 2. Clear AQP-4 antibody status record at enrollment; 3. Treated with satralizumab and completed 3 induction treatments; 4. Follow-up of >=6 months, and can provide clear prognosis or relapse information.

Exclusion criteria

Exclusion criteria: 1. Both serum and cerebrospinal fluid AQP-4 antibodies are negative; 2. Serum or cerebrospinal fluid MOG antibodies are positive; 3. Prior concomitant medication: received B cell depletion agents within 6 months before baseline (excluding cases where B cells have returned to normal levels) or IL-6 receptor antagonists within 2 months; received other immunosuppressive therapy before baseline within the expected pharmacodynamics effect window; 4. Key data missing; 5. Refused follow-up and assessment.

Design outcomes

Primary

MeasureTime frame
Annual recurrence rate, ARR;Expanded Disability Status Scale, EDSS;

Secondary

MeasureTime frame
IL-6;immune globulin G;

Countries

China

Contacts

Public ContactSongdi Wu

Xi'an No.1 Hospital

wusongdi@gmail.com+86 186 2926 5635

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026