New project aims to sharpen diagnosis of rare kidney diseases
NCT ID NCT05985122
First seen Nov 01, 2025 · Last updated Apr 24, 2026 · Updated 23 times
Summary
This study is part of a European project to improve how doctors diagnose and monitor two rare kidney diseases: aHUS and C3G. Researchers will develop new lab tests and study blood, cells, and kidney tissue from 180 patients and healthy volunteers. The goal is to find better markers to guide personalized treatment with complement-blocking drugs.
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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.
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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Locations
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Centro di Ricerche Cliniche per le Malattie Rare "Aldo e Cele Daccò"
Ranica, BG, 24020, Italy
Conditions
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