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NCT01522183 · ClinicalTrials.gov registry record

Atypical Hemolytic-Uremic Syndrome (aHUS) Registry

A clinical trial of Atypical Hemolytic-Uremic Syndrome, sponsored by Alexion Pharmaceuticals.

Recruiting
Registry status
3,000
Enrollment target
20
Study locations

NCT01522183 is a study of Atypical Hemolytic-Uremic Syndrome that is actively recruiting participants, run by Alexion Pharmaceuticals. The registered enrollment target is 3,000 participants, above the 53-participant average among 3 other Atypical Hemolytic-Uremic Syndrome trials with a reported enrollment target (5560% higher). The trial reports 20 study locations across 14 states.

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The verdict

NCT01522183, a study of Atypical Hemolytic-Uremic Syndrome, is actively recruiting participants, sponsored by Alexion Pharmaceuticals.

RECRUITING
Registry status
3,000 participants
Enrollment target
20
Study locations

Study Summary

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

Study Locations (20)

Queensland

  • Clinical Trial Site - Cairns
  • Clinical Trial Site - Herston
  • Clinical Trial Site - Woolloongabba

Victoria

  • Clinical Trial Site - Heidelberg
  • Clinical Trial Site - Parkville
  • Clinical Trial Site - Parkville

New South Wales

  • Clinical Trial Site 1 - Westmead
  • Clinical Trial Site 2 - Westmead

Western Australia

  • Clinical Trial Site - Murdoch
  • Clinical Trial Site - Nedlands

Colorado

  • Clinical Trial Site - Aurora

District of Columbia

  • Clinical Trial Site - Washington D.C.

Florida

  • Clinical Trial Site - Gainesville

Georgia

  • Clinical Trial Site - Atlanta

Trial Details

FieldValue
Enrollment Target 3,000 participants
Start Date 2013-03-18
Est. Completion 2031-01-01

Sponsor

Alexion Pharmaceuticals

162 total trials

What the Registry Record Tells You About NCT01522183

The ClinicalTrials.gov registry entry for NCT01522183 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 3,000 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 53-participant average among 3 other Atypical Hemolytic-Uremic Syndrome trials with a reported enrollment target (5560% higher). The listed sponsor is Alexion Pharmaceuticals, which has 162 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Atypical Hemolytic-Uremic Syndrome appearing as the primary indexed condition, and to 0 interventions.

NCT01522183 reports 20 study locations spanning 14 distinct geographic areas - top geographies include Queensland, Victoria, New South Wales.

Frequently Asked Questions

What is clinical trial NCT01522183 about?

NCT01522183 is a clinical study titled "Atypical Hemolytic-Uremic Syndrome (aHUS) Registry". Post-marketing safety data on patients treated and untreated with eculizumab or ravulizumab.

What is the current status of trial NCT01522183?

This trial is currently recruiting. The enrollment target is 3,000 participants. The study started on 2013-03-18. Estimated completion is 2031-01-01.

What conditions does trial NCT01522183 study?

This clinical trial studies the following conditions: Atypical Hemolytic-Uremic Syndrome.

Who is sponsoring clinical trial NCT01522183?

This trial is sponsored by Alexion Pharmaceuticals, which has 162 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01522183 being conducted?

This trial has 20 study locations across Colorado, District of Columbia, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.