atypical Hemolytic-Uremic Syndrome (aHUS) Registry

Study identifier:M11-001

ClinicalTrials.gov identifier:NCT01522183

EudraCT identifier:N/A

CTIS identifier:N/A

Recruiting

Official Title

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

Medical condition

Atypical Hemolytic-Uremic Syndrome

Phase

Phase 4

Healthy volunteers

No

Study drug

-

Sex

All

Estimated Enrollment

3000

Study type

Observational

Age

n/a - n/a

Date

Study Start Date: 26 Apr 2012
Estimated Primary Completion Date: 01 Jan 2031
Estimated Study Completion Date: 01 Jan 2031

Study design

Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Jun 2024 by Alexion Pharmaceuticals, Inc.

Sponsors

Alexion Pharmaceuticals, Inc.

Collaborators

SyneosHealth

Inclusion and exclusion criteria