A Clinical Research Study of Inebilizumab in Neuromyelitis Optica Spectrum Disorders
NCT06212245 · Status: NOT_YET_RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 33
Last updated 2024-01-18
Summary
To assess the efficacy and safety of Inebilizumab in Chinese adult patients with neuromyelitis optica spectrum disorders.
Conditions
- Neuromyelitis Optica Spectrum Disorders
Interventions
- DRUG
-
Inebilizumab
Participants will receive IV inebilizumab 300 mg
Sponsors & Collaborators
-
Horizon Therapeutics Ireland DAC
collaborator INDUSTRY -
Hansoh BioMedical R&D Company
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-02-25
- Primary Completion
- 2024-12-25
- Completion
- 2025-06-25
Countries
- China
Study Locations
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