Sugar clues in rare disease: new study seeks to unlock AL amyloidosis mysteries
NCT ID NCT07448779
First seen Mar 10, 2026 · Last updated May 23, 2026 · Updated 6 times
Summary
This study aims to understand how a specific sugar modification (N-glycosylation) on abnormal proteins contributes to AL amyloidosis, a rare disease where these proteins build up and damage organs. Researchers will analyze blood and bone marrow samples from 100 adults with related conditions like AL amyloidosis or MGUS. The goal is to improve diagnosis, risk assessment, and potentially find new treatment targets.
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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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Contacts and locations
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Locations
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Fondazione IRCCS Policlinico San Matteo di Pavia
RECRUITINGPavia, PV, 27100, Italy
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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