RecruitingPhase 3NMOSDNCT07557420

What it found

Still running

No result yet.

What was tested

Treatment tested

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 progression
  • Change 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

    Safety
  • Serum 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 response
  • Number 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 registry

About 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

    1. Started

      Jul 2026

    2. Main results due

      Sept 2028

    3. Finished

      Sept 2028

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