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.
At the time of enrollment in the Registry, participant records will be queried for retrospective information about the participant's medical history and AQP4+ NMOSD treatment history for the time period beginning 1 year prior to ALXN-C5IT initiation through Registry enrollment. The duration of data collection for the Registry will be approximately 5 years from the day the last participant is enrolled.
Study Type
OBSERVATIONAL
Enrollment
122
Clinical Trial Site
Washington D.C., District of Columbia, United States
RECRUITINGResearch Site
Boston, Massachusetts, United States
RECRUITINGClinical Trial Site
Chapel Hill, North Carolina, United States
NOT_YET_RECRUITINGClinical Trial Site
Columbus, Ohio, United States
Annualized Relapse Rate (ARR)
The ARR is defined as the total number of relapses divided by the total number of participant-years.
Time frame: Up to approximately 5 years
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Clinical Trial Site
Plano, Texas, United States
RECRUITINGClinical Trial Site
Milwaukee, Wisconsin, United States
RECRUITINGClinical Trial Site
Buenos Aires, Argentina
RECRUITINGClinical Trial Site
Buenos Aires, Argentina
NOT_YET_RECRUITINGClinical Trial Site
Buenos Aires, Argentina
RECRUITINGClinical Trial Site
Buenos Aires, Argentina
RECRUITING...and 23 more locations