Efficacy, Safety, Pharmacokinetics, Pharmacodynamics, and Immunogenicity Study of Ravulizumab in Chinese Adults With Neuromyelitis Optica Spectrum Disorder (NMOSD)
What it found
No result yet.
What was tested
Treatment tested
- Ravulizumab
Complement C5 inhibitor
What it measured
Main measures
Adjudicated On-Trial Annualized Relapse Rate (ARR)
Baseline up to Week 50
Relapses
Other measures (9)
Number of Participants With Clinically Important Change From Baseline in Hauser Ambulation Index (HAI) Score
Baseline up to Week 50
Number of Participants With Clinically Important Worsening From Baseline in Expanded Disability Status Scale (EDSS) Score
Baseline up to Week 50
Disability progressionChange From Baseline in European Quality of Life Health 5-item Questionnaire (EQ-5D) Index Score
Baseline, Week 50
Quality of life (reported by participants)Change From Baseline in EQ-5D Visual Analog Scale (VAS) Score
Baseline, Week 50
Quality of life (reported by participants)Number of Participants With Treatment Emergent Adverse Events (TEAEs), Treatment Emergent Serious Adverse Events (TESAEs) and Adverse Events of Special Interests (AESIs)
Baseline up to Week 50
SafetySerum Ravulizumab Concentration
Day 1 to Day 351
Change From Baseline in Serum Free Complement Component 5 (C5) Concentration
Baseline Up to Day 351
Number of Participants With Anti-Drug Antibodies (ADAs)
Day 1 up to Day 351
Immune responseNumber of Participants With Neutralizing Antibodies (NAb)
Day 1 up to Day 351
Immune response
Who could take part
NMOSD · 18 to 130
Key Inclusion (essential) * Diagnosis: NMOSD per 2015 international consensus criteria, and anti AQP4 antibody positive at Screening. * Disease activity: ≥1 attack/relapse in the past 12 months. * Disability: EDSS ≤7. * Background therapy: If on IST and/or oral corticosteroids, participant should be on a stable maintenance regimen prior to Screening and plan to remain stable during the study unless relapse occurs. (Detailed agent specific duration/dose rules to be confirmed at screening.) * Body weight: ≥40 kg. * Vaccinated against meningococcal infections from serogroups A, C, W, Y (and B where available) within the 3 years prior to study intervention administration on Day 1. Key Exclusion (essential) * Pregnancy/lactation: Pregnant, breastfeeding, or intending to conceive during the study. * Infection risk: History of meningococcal disease or unresolved meningococcal disease, active systemic infection within 14 days, or fever ≥38°C within 7 days before Day 1. * Hypersensitivity: To murine proteins or ravulizumab excipients. * Serious comorbidities: Any condition that in the Investigator's judgment adds risk or interferes with participation/assessment. * Viral infections: Known HIV, active HBV, or active HCV. * Prior/concomitant immunomodulatory treatments: * B cell-depleting therapy (e.g., rituximab, inebilizumab) within 3 months before Screening. * Mitoxantrone or satralizumab within 3 months before Screening. * IVIg within 3 weeks before Screening. * Any prior or current complement inhibitor. Note: Other protocol-defined criteria may apply and should be verified during full eligibility review.
As registered. Criteria can change, so ask the trial team or your neurologist.
Contact details on the registryAbout this trial
In the sponsor's words
The primary objective of this study is to confirm the efficacy, safety, pharmacokinetics (PK), pharmacodynamics (PD), and immunogenicity of ravulizumab in the treatment of Chinese adults with anti-aquaporin-4 (AQP4) antibody (Ab) + neuromyelitis optica spectrum disorder (NMOSD).
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History
Started
Jul 2026
Main results due
Sept 2028
Finished
Sept 2028
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