Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT05891379

Inebilizumab in Acute Neuromyelitis Optica Spectrum Disorders

Sponsor: Xuanwu Hospital, Beijing

View on ClinicalTrials.gov

Summary

This study is aimed to observe the effectiveness and safety of inebilizumab in the acute phase of neuromyelitis optica spectrum disorders.

Official title: Effectiveness and Safety of Inebilizumab in the Acute Phase of Neuromyelitis Optica Spectrum Disorders-a Multicentric, Prospective, Real Word Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2024-07-09

Completion Date

2025-07-31

Last Updated

2024-09-19

Healthy Volunteers

No

Interventions

DRUG

Inebilizumab

Inebilizumab: 300mg IV on Day1 and Day 15. The first dose of inelizumab is given during IVMP.

DRUG

oral immunosuppressant

Oral immunosuppressants (azathioprine or mycolate mofetil) are initiated during IVMP.

Locations (1)

Xuanwu Hospital, Capital Medical University

Beijing, Beijing Municipality, China