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Cost-effectiveness analysis of satralizumab, inebilizumab, and mycophenolate mofetil for neuromyelitis optica spectrum disorder: a multicenter retrospective real-world study based on registry cohort and national health insurance data

Cost-effectiveness analysis of satralizumab, inebilizumab, and mycophenolate mofetil for neuromyelitis optica spectrum disorder: a multicenter retrospective real-world study based on registry cohort and national health insurance data

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128384
Enrollment
Unknown
Registered
2026-07-20
Start date
2026-07-20
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Aquaporin-4 (AQP4) antibody-positive neuromyelitis optica spectrum disorder

Interventions

Observation group:None

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients meeting the 2015 International Panel for NMO Diagnosis (IPND) criteria for NMOSD; 2.Seropositive for AQP4-IgG, detected by cell-based assay (CBA) or other methods validated by the investigators as reliable; 3.Received >=1 dose of satralizumab (SAT), inebilizumab (INE), or mycophenolate mofetil (MMF); 4.Have verifiable diagnostic and treatment records; 5.Completed at least one follow-up visit after treatment initiation; 6.Possess relatively complete clinical data required for the study; 7.Identifiable within the national health insurance reimbursement database;

Exclusion criteria

Exclusion criteria: 1.Patients with severe organ dysfunction or concomitant active autoimmune diseases; 2.Myelin oligodendrocyte glycoprotein immunoglobulin G (MOG-IgG) seropositivity; 3.Significant missing data in key clinical or cost variables; 4.Treatment switching during follow-up (to be addressed via sensitivity analysis or censoring);

Design outcomes

Primary

MeasureTime frame
time to first protocol-defined relapse;

Secondary

MeasureTime frame
annualized relapse rate;

Countries

China

Contacts

Public ContactYan Xu

Peking Union Medical College Hospital

xuyanpumch@hotmail.com+86 10 69156371

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026