Study identifier:D928BR00003
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A non-interventional study evaluating ravulizumab treatment outcomes in Polish patients with Atypical Hemolytic Uremic Syndrome
Atypical Hemolytic Uremic Syndrome
-
no
Ravulizumab
All
80
Observational
18 Years +
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Jan 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Prospective cohort Group of patients naive to complement inhibitors | Drug: Ravulizumab Ultomiris |
| Retrospective cohort Group of patients who transitioned from other complement inhibitors to ravulizumab. | Drug: Ravulizumab Ultomiris |