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A survey of treatment practice for patients with neuromyelitis optica spectrum disorder under satralizumab treatment using Japanese claims database

Not Applicable
Conditions
neuromyelitis optica spectrum disorder (NMOSD)
Registration Number
JPRN-UMIN000049131
Lead Sponsor
CHUGAI PHARMACEUTICAL CO.,LTD.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of patients who reduced oral corticosteroid to 0 mg at day 360 without relapse under continuous satralizumab prescription
Secondary Outcome Measures
NameTimeMethod
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