🔎 Trials Near Me

Home › NCT01522183

Atypical Hemolytic-Uremic Syndrome (aHUS) Registry

RecruitingObservational study

An Observational, Non-Interventional, Multi-Center, Multi-National Study of Patients With Atypical Hemolytic-Uremic Syndrome (aHUS Registry)

Who can join

All ages · All sexes

Full eligibility criteria
Inclusion Criteria:

* Male or female patients of any age, including minors, who have been diagnosed with aHUS
* Patients with or without an identified complement pathogenic variant or anti-complement factor antibody
* Able to give written informed consent. Patient or patient's parent/legal guardian must be willing and able to given written informed consent and the patient (if minor) must be willing to give written informed assent \[if applicable as determined by the central Institutional Review Boards/Independent Ethics Committees (IRB/IEC)\].
* ADAMTS13 \> 5%, if performed.

Exclusion Criteria:

* Hemolytic Uremic Syndrome (HUS) only due to Shiga Toxin producing Escherichia coli (STEC).
* Unable to give written informed consent. Patient or patient's parent/legal guardian unable to give written informed consent. Patient (if minor) unable to give written informed assent (if applicable as determined by the central Institutional Review Boards/Independent Ethics Committees \[IRB/IEC\]).

About the study

Post-marketing safety data on patients treated and untreated with eculizumab or ravulizumab.

Sponsor: Alexion Pharmaceuticals, Inc. · Participants: 3,000 · Started: Mar 18, 2013

Contact the study team

Official record on ClinicalTrials.gov — NCT01522183

Locations in the U.S.

ColoradoClinical Trial Site, Aurora
District of ColumbiaClinical Trial Site, Washington D.C.
FloridaClinical Trial Site, Gainesville
GeorgiaClinical Trial Site, Atlanta
MassachusettsClinical Trial Site, Boston
MissouriClinical Trial Site, St Louis

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.