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| ID | Type | Description | Link |
|---|---|---|---|
| ALXN1210-NMO-324 | Other Identifier | Alexion |
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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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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ravulizumab | Experimental | Participants will receive a weight-based loading dose of ravulizumab on Day 1, followed by a weight-based maintenance treatment dose on Day 15 and every 8 weeks (q8w) thereafter for up to 50 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ravulizumab | Drug | Participants will receive ravulizumab via intravenous (IV) infusion. |
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| Measure | Description | Time Frame |
|---|---|---|
| Adjudicated On-Trial Annualized Relapse Rate (ARR) | Baseline up to Week 50 |
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
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Key Inclusion (essential)
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:
Note: Other protocol-defined criteria may apply and should be verified during full eligibility review.
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Alexion Pharmaceuticals, Inc. (Sponsor) | Contact | 1-855-752-2356 | clinicaltrials@alexion.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research Site | Chengdu | 610016 | China | |||
| Research Site |
Alexion has a public commitment to allow requests for access to study data and will be supplying a protocol, CSR, and plain language summaries.
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| Baseline up to Week 50 |
| Change From Baseline in European Quality of Life Health 5-item Questionnaire (EQ-5D) Index Score | Baseline, Week 50 |
| Change From Baseline in EQ-5D Visual Analog Scale (VAS) Score | Baseline, Week 50 |
| 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 |
| 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 |
| Number of Participants With Neutralizing Antibodies (NAb) | Day 1 up to Day 351 |
| Dongguan |
| 523059 |
| China |
| Research Site | Shanghai | 201107 | China |
| Research Site | Wenzhou | 325000 | China |
| Research Site | Wuhan | 430030 | China |
| ID | Term |
|---|---|
| D009471 | Neuromyelitis Optica |
| ID | Term |
|---|---|
| D009188 | Myelitis, Transverse |
| D020278 | Demyelinating Autoimmune Diseases, CNS |
| D020274 | Autoimmune Diseases of the Nervous System |
| D009422 | Nervous System Diseases |
| D009902 | Optic Neuritis |
| D009901 | Optic Nerve Diseases |
| D003389 | Cranial Nerve Diseases |
| D003711 | Demyelinating Diseases |
| D005128 | Eye Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
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| ID | Term |
|---|---|
| C000629409 | ravulizumab |
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