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

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06212245 on ClinicalTrials.gov