Atypical Hemolytic-Uremic Syndrome (aHUS) Registry
Atypical Hemolytic-Uremic SyndromePost-marketing safety data on patients treated and untreated with eculizumab or ravulizumab.
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Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
0 and up
Critères de participation
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 \[IRB/IEC\]).
Lieu de l'étude
Clinical Trial Site
Clinical Trial SiteToronto, Ontario
Canada
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Licht
Clinical Trial Site
Clinical Trial SiteLondon, Ontario
Canada
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Huang
Clinical Trial Site
Clinical Trial SiteMontréal, Quebec
Canada
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Lapeyraque
Clinical Trial Site
Clinical Trial SiteQuébec, Quebec
Canada
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Philibert
- Étude parrainée par
- Alexion Pharmaceuticals, Inc.
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT01522183