🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT05966467
Recruiting Observational

Registry of Patients With AQP4+ NMOSD Treated With Alexion C5 Inhibitor Therapies

NCT05966467 · tracked via the Priya Life Science USA tracker
Sponsor
Alexion Pharmaceuticals, Inc.
Phase
Observational
Started
2024-02-01
Last updated
2026-06-18

Condition(s) studied

Neuromyelitis Optica Spectrum DisorderNMOSDAQP4+ NMOSD

Study summary

Long-term, multicenter, multinational, observational, registry of patients with AQP4+ NMOSD that is designed to collect data on clinical outcomes and safety in patients prescribed Alexion C5 inhibitor therapies (C5IT). The registry will also collect data on patient reported outcomes (PROs), quality of life (QoL), and targeted AQP4+ NMOSD therapies used to provide evidence on the real-world impact of ALXN-C5IT on patients with AQP4+ NMOSD.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Participant is ≥ 18 years of age at the time of enrollment in the Registry. * Participant must have a confirmed diagnosis of AQP4+ NMOSD. * At the time of enrollment in the Registry, participants must be receiving treatment with ALXN-C5IT for the purpose of chronic relapse prevention in a manner consistent with the local label. Specifically, they should have received at least 1 dose of eculizumab within 4 weeks prior to enrollment or at least 1 dose of ravulizumab within 12 weeks prior to enrollment. * Participants must have both the following historical data available to be enrolled in the Registry: ALXN-C5IT dosing information since initiation and number and types of relapses from 1 year prior to ALXN-C5IT initiation through Registry enrollment. Exclusion Criteria: * Participants currently enrolled in an interventional clinical study for the treatment of AQP4+ NMOSD in which the intervention is a drug.

Primary outcome measure(s)

Trial sites (33)

FacilityCityRegionStatus
Clinical Trial Site Washington D.C. District of Columbia Recruiting
Research Site Boston Massachusetts Recruiting
Clinical Trial Site Chapel Hill North Carolina Not Yet Recruiting
Clinical Trial Site Columbus Ohio Recruiting
Clinical Trial Site Plano Texas Recruiting
Clinical Trial Site Milwaukee Wisconsin Recruiting
Clinical Trial Site Buenos Aires Argentina Recruiting
Clinical Trial Site Buenos Aires Argentina Not Yet Recruiting
Clinical Trial Site Buenos Aires Argentina Recruiting
Clinical Trial Site Buenos Aires Argentina Recruiting
Clinical Trial Site Burnaby British Columbia Recruiting
Clinical Trial Site Beijing China Not Yet Recruiting
Clinical Trial Site Guangzhou China Not Yet Recruiting
Clinical Trial Site Henan China Not Yet Recruiting
Clinical Trial Site Shanghai China Not Yet Recruiting
Clinical Trial Site Sichuan China Not Yet Recruiting
Clinical Trial Site Wuhan China Not Yet Recruiting
Clinical Trial Site Dresden Germany Recruiting
Clinical Trial Site Essen Germany Recruiting
Clinical Trial Site München Germany Not Yet Recruiting
Clinical Trial Site Naples Italy Recruiting
Clinical Trial Site Fukuoka Japan Recruiting
Clinical Trial Site Kawasaki Japan Recruiting
Clinical Trial Site Miyagi Japan Recruiting
Clinical Trial Site Tokyo Japan Not Yet Recruiting
Clinical Trial Site Daejeon South Korea Recruiting
Clinical Trial Site Gyeonggi-do South Korea Recruiting
Clinical Trial Site Seoul South Korea Recruiting
Clinical Trial Site Seoul South Korea Recruiting
Clinical Trial Site Seoul South Korea Recruiting
Clinical Trial Site Seoul South Korea Recruiting
Clinical Trial Site Seoul South Korea Recruiting
Clinical Trial Site Seoul South Korea Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05966467 on ClinicalTrials.gov ↗ ← All trials in the USA