Massive european study aims to unlock secrets of rare kidney disease

NCT ID NCT05927467

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study follows 700 people with Alport syndrome, a rare inherited disease that can lead to kidney failure, hearing loss, and eye problems. Researchers will collect health data and samples over time to map how the disease progresses and to find early markers of kidney decline. The goal is to better understand the disease and prepare for future treatment trials.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this study could reveal early warning signs of kidney failure in Alport syndrome, helping doctors start treatments sooner and guiding the design of future drug trials.

What could go wrong

This is an observational study, not a treatment trial. It will not directly improve health, and results may take years to produce clear findings.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Conditions

The condition(s) this trial relates to.

Alport syndrome hereditary nephritis kidney disorder Rare Diseases

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • RaDiCo Eurbio-Alport

    RECRUITING

    Paris, Île-de-France Region, 75012, France

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••