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Efficacy and Safety Study of Ravulizumab IV in Pediatric Participants With NMOSD
Sponsor: Alexion Pharmaceuticals, Inc.
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).
Official title: A Phase 2/3, Open-label, Historical-controlled, Single-arm, Multicenter Study to Evaluate the Efficacy, Pharmacokinetics, Pharmacodynamics, and Safety of Ravulizumab in Children and Adolescents With Aquaporin-4 Antibody Positive (AQP4-Ab [+]) Neuromyelitis Optica Spectrum Disorder (NMOSD)
Key Details
Gender
All
Age Range
Any - Any
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2022-06-23
Completion Date
2029-04-02
Last Updated
2025-11-12
Healthy Volunteers
No
Conditions
Interventions
Ravulizumab
Participants will receive a weight-based loading dose of ravulizumab on Day 1, followed by weight-based maintenance treatment with ravulizumab on Day 15 and every 8 weeks (q8w) after or once every 4 weeks (q4w) depending on weight. During the Extension Period, participants will continue to receive weight-based maintenance doses of ravulizumab IV on Day 351 and q8w or q4w, depending on weight.
Locations (21)
Research Site
Washington D.C., District of Columbia, United States
Research Site
Miami, Florida, United States
Research Site
Boston, Massachusetts, United States
Research Site
St Louis, Missouri, United States
Research Site
Durham, North Carolina, United States
Research Site
Philadelphia, Pennsylvania, United States
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Edmonton, Alberta, Canada
Research Site
Toronto, Ontario, Canada
Research Site
Montreal, Quebec, Canada
Research Site
Le Kremlin-Bicêtre, France
Research Site
Marseille, France
Research Site
Montpellier, France
Research Site
Bochum, Germany
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Giessen, Germany
Research Site
Catania, Italy
Research Site
Chieti, Italy
Research Site
Gallarate, Italy
Research Site
Roma, Italy
Research Site
Yokohama, Japan
Research Site
Goyang-si, South Korea
Research Site
Esplugues de Llobregat, Spain