MedPath

Efficacy and Safety Study of Ravulizumab IV in Pediatric Participants With NMOSD

Phase 2
Recruiting
Conditions
Neuromyelitis Optica Spectrum Disorder
Interventions
Registration Number
NCT05346354
Lead Sponsor
Alexion Pharmaceuticals, Inc.
Brief Summary

The primary purpose of this study is to evaluate the safety and efficacy of ravulizumab in pediatric participants with Neuromyelitis Optica Spectrum Disorder (NMOSD).

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
12
Inclusion Criteria
  • Participants must be anti-AQP4 Ab-positive and have a diagnosis of NMOSD as defined by the 2015 international consensus diagnostic criteria.
  • Complement inhibitor treatment-naïve participants must have had at least 1 attack or relapse in the last 12 months prior to the Screening Period.
  • Expanded Disability Status Scale (EDSS) score ≤ 7.
  • Eculizumab-experienced participants must be clinically stable per Investigator for 30 days and have been treated with eculizumab in Study ECU-NMO-303 for at least 90 days prior to screening with no missed doses within 2 months prior to Day 1.
  • Participants who enter the study receiving supportive IST(s) (eg, corticosteroid, azathioprine [AZA], mycophenolate mofetil [MMF], methotrexate [MTX], tacrolimus [TAC], cyclosporin [CsA], or cyclophosphamide [CYC]) for the prevention of relapse, either in combination or monotherapy, must be on a stable dosing regimen of adequate duration prior to Screening and remain on a stable dosing regimen during the Screening Period.
  • To reduce the risk of meningococcal infection (Neisseria meningitidis), all participants must be vaccinated against meningococcal infection.
  • Documented vaccination for Hib and S pneumoniae at least 14 days prior to Day 1 according to national/local guidelines for the applicable age group.
Exclusion Criteria
  • Use of rituximab within 3 months prior to screening.
  • Currently treated with a biologic medications (other than eculizumab) that may affect immune system functioning, or has stopped treatment with a biologic medication that may affect immune system functioning, and 5 half lives of the medication have not elapsed by the time of the Screening Visit.
  • Use of intravenous immunoglobulin (IVIg) or plasma exchange (PE) within 3 weeks prior to Screening.
  • Participation in another investigational drug or investigational device study (other than Study ECU-NMO-303) within 5 half lives of that investigational product (if known) or 30 days before initiation of the first dose of study drug, whichever is longer.
  • Use of immunomodulatory therapies for multiple sclerosis within 3 months prior to Screening.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
RavulizumabRavulizumabDuring the Primary Treatment Period, all participants will receive weight-based dosing of ravulizumab IV for a total of 50 weeks of treatment. During the Extension Period, participants will continue to receive weight-based dosing of ravulizumab IV for up to 104 weeks.
Primary Outcome Measures
NameTimeMethod
Change From Baseline in the Annualized Relapse Rate at Week 50Baseline, Week 50
Time to First Adjudicated On-trial Relapse through Week 50Baseline through Week 50
Secondary Outcome Measures
NameTimeMethod
Change From Baseline in Confrontational Visual Fields at Week 50Baseline, Week 50
Change From Baseline in Expanded Disability Status Scale Score At Week 50Baseline, Week 50

The score ranges are 0 to 10, higher score indicates worse outcome.

Change from Baseline in Free Serum Complement Component 5 (C5) Concentration Over Time Through Week 50Baseline through Week 50
Change From Baseline in Hauser Ambulation Index at Week 50Baseline, Week 50

The score ranges are 0 to 9, higher score indicates worse outcome.

Change From Baseline in Visual Acuity at Week 50Baseline, Week 50
Change From Baseline in Color Vision at Week 50Baseline, Week 50
Serum Ravulizumab ConcentrationPredose and postdose (at end of infusion) on Day 1, Weeks 2, 10, 18, 26, and 42, and predose on Week 50

Trial Locations

Locations (1)

Research Site

🇪🇸

Esplugues de Llobregat, Spain

© Copyright 2025. All Rights Reserved by MedPath