Study identifier:HEMRAV601IT
ClinicalTrials.gov identifier:NCT05274633
EudraCT identifier:N/A
CTIS identifier:N/A
Real Life Use of Ravulizumab in Italian Patients with Paroxysmal Nocturnal Hemoglobinuria a Multicenter Observational Retrospective and Prospective Cohort Study.
paroxysmal nocturnal hemoglobinuria
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No
Ravulizumab
All
120
Observational
18 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Apr 2024 by Alexion Pharmaceuticals, Inc.
Alexion Pharmaceuticals, Inc.
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No locations available
Arms | Assigned Interventions |
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Participants With PNH Data will be collected on participants who were already treated with eculizumab for at least 26 weeks and who started ravulizumab treatment as per clinical practice. | - |