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Ravulizumab Outcomes in Polish Patients With aHUS

RecruitingN/A

Sponsor: AstraZeneca

Conditions: Atypical Hemolytic Uremic Syndrome

Interventions: Ravulizumab

Countries: Poland

This multicenter, observational cohort study uses retrospective collection of past medical history and prospective follow-up to capture longitudinal data on the management and clinical outcomes of patients with atypical hemolytic uremic syndrome (aHUS) treated with ravulizumab as part of routine clinical practice under Poland's National Drug Program (NDP).

Eligibility overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* Patients of all ages diagnosed with atypical hemolytic uremic syndrome (aHUS) who received treatment with ravulizumab under the National Drug Program (NDP) in Poland.
* Patients who are willing to participate in the study and have provided informed consent by signing the informed consent form (ICF).

Exclusion Criteria:

* Individuals who intend to participate in a clinical trial for atypical hemolytic uremic syndrome (aHUS) on or after the date of their first ravulizumab infusion through the National Drug Program.
* Patients with cognitive impairments, those who are unwilling to participate, or those facing language barriers that hinder adequate comprehension or cooperation.

Locations (10)

Gdansk, Poland
Katowice, Poland
Katowice, Poland
Krakow, Poland
Lodz, Poland
Poznan, Poland
Warsaw, Poland
Warsaw, Poland
Wroclaw, Poland
Wroclaw, Poland