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Atypical Hemolytic-Uremic Syndrome (aHUS) Registry

This study, called the Atypical Hemolytic-Uremic Syndrome (aHUS) Registry, is designed to collect important safety information after new medicines like eculizumab and ravulizumab have been approved and are being used by patients. It helps doctors understand how safe these treatments are in real-world use. The study also tracks how aHUS affects patients over time, regardless of whether they are on these specific treatments or not. It's open to people of all ages, including children, who have been diagnosed with aHUS. The main goal is to improve our understanding of aHUS and its treatments to help future patients.

At a glance

Status
Recruiting
Sponsor
Alexion Pharmaceuticals, Inc.
Enrolment target
3,000
Start
18 Mar 2013
Estimated completion
01 Jan 2031

What is this study about?

This registry is a study for people with a rare kidney condition called atypical Hemolytic-Uremic Syndrome, or aHUS. When new medicines are approved, doctors need to keep learning how they work in real life. This study collects information on patients who are treated with two specific medicines, eculizumab or ravulizumab, to see how safe they are once they've been approved and are being used widely. This is called 'post-marketing safety data'.

But it's not just about these medicines. The study also collects details on how aHUS affects patients over time, no matter what treatment they are receiving, or even if they aren't on these particular medicines. This helps doctors and researchers understand the condition better and how it progresses in different people.

By gathering this information from many patients, researchers hope to get a clearer picture of aHUS and how best to manage it. This can lead to better care and understanding for everyone affected by this rare disease in the future.

Key takeaways

  • It's a study about a rare kidney disease called aHUS.
  • It collects information on how aHUS progresses and how safe certain medicines are.
  • Participation involves sharing medical information, not new treatments.
  • It's open to patients of all ages, including children.
  • The goal is to improve understanding and care for aHUS patients.

Who may be eligible?

You might be able to join this study if you've been diagnosed with atypical Hemolytic-Uremic Syndrome (aHUS). This includes people of all ages, from young children to adults. It doesn't matter if doctors have found a specific genetic cause for your aHUS or not.

An important part of joining is being able to understand and sign a consent form. If you're under 18, your parent or legal guardian would sign for you, and you would also be asked if you're happy to take part.

You would not be able to join if your Hemolytic Uremic Syndrome (HUS) is only caused by a specific type of E. coli bacteria (Shiga Toxin producing E. coli). Also, if you or your guardian are unable to give written consent, then you would not be able to take part.

Could this study suit you?

Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.

  1. I have been diagnosed with atypical Hemolytic-Uremic Syndrome (aHUS).
  2. My HUS is not caused only by a specific E. coli infection.
  3. I (or my parent/guardian if I'm under 18) can understand and give written permission to take part.
  4. If I'm under 18, I am happy to take part myself.
Answer every question to see your result.

What does participation involve?

This study is a registry, which means it mainly involves collecting information about your condition and treatment from your medical records. You would continue to receive your usual medical care from your own doctors. There are no specific study visits or extra medication given as part of this registry. Your treatment decisions would be made by you and your doctor as normal. The study would gather information over a period of time, tracking your health and any treatments you receive for aHUS.

Potential risks and benefits

Taking part in this study may not directly benefit you, but the information collected will help doctors and researchers better understand aHUS and its treatments for future patients. This could lead to improved care for others. There are very few direct risks to participating, as it primarily involves collecting information from your medical records. Your medical care would not change. You are always free to decide to stop participating in the study at any time without it affecting your medical care.

Locations (141)

Some site locations are approximate. We're improving this — please verify with the trial team before travelling.
  • Clinical Trial Site
    Verified postcode
    Aurora, United States· Recruiting
  • Clinical Trial Site
    Verified postcode
    Washington D.C., United States· Recruiting
  • Clinical Trial Site
    Verified postcode
    Gainesville, United States· Recruiting
  • Clinical Trial Site
    Verified postcode
    Atlanta, United States· Recruiting
  • Clinical Trial Site
    Verified postcode
    Chicago, United States· Withdrawn
  • Clinical Trial Site
    Verified postcode
    Boston, United States· Recruiting
  • Clinical Trial Site
    Verified postcode
    St Louis, United States· Recruiting
  • Clinical Trial Site
    Verified postcode
    Winston-Salem, United States· Withdrawn
  • Clinical Trial Site
    Verified postcode
    Columbus, United States· Active not recruiting
  • Clinical Trial Site 1
    Verified postcode
    Westmead, Australia· Recruiting
  • Clinical Trial Site 2
    Verified postcode
    Westmead, Australia· Recruiting
  • Clinical Trial Site
    Verified postcode
    Cairns, Australia· Recruiting

Common questions

What is atypical Hemolytic-Uremic Syndrome (aHUS)?

It's a very rare and serious kidney disease that can damage blood vessels.

Will I get new medicine in this study?

No, this study only collects information about your current medical care and treatments.

Who can join this study?

People of all ages diagnosed with aHUS, as long as it's not caused by a specific E. coli infection.

What information will the study collect?

It will gather details about your aHUS, its progression, and any treatments you receive.

Can I leave the study if I change my mind?

Yes, you can withdraw from the study at any time without affecting your medical care.

How to find out more

Alexion Pharmaceuticals, Inc. (Sponsor)

Always speak to your GP or specialist before deciding to take part in a study.

Interested in taking part?

Register your interest

Share your details and the research team for "Atypical Hemolytic-Uremic Syndrome (aHUS) Registry…" will contact you if you may be eligible. Always speak to your GP before agreeing to take part.

Discussion

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