Protein clues could spot rare disease years early

NCT ID NCT03431896

First seen Feb 28, 2026 · Last updated Jun 19, 2026 · Updated 21 times

Summary

This study followed 37 people with a genetic risk for hereditary ATTR amyloidosis over five years. Researchers measured levels of misfolded proteins in the blood to see if they could detect the earliest signs of the disease. The goal is to develop a way to catch the condition before symptoms appear, potentially allowing for earlier treatment.

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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for AMYLOIDOSIS are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Locations

  • Cleveland Clinic

    Cleveland, Ohio, 44195, United States

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 could lead to a blood test that catches ATTR amyloidosis earlier, allowing for timely treatment.

What could go wrong

This is a small observational study (37 people) that only measures a biomarker, not a treatment. The protein changes may not reliably predict disease onset in all patients.

Conditions

The condition(s) this trial relates to.

AL amyloidosis Alzheimer disease Amyloid Neuropathies, Familial amyloidosis familial amyloid neuropathy Immunoglobulin Light-chain Amyloidosis restrictive cardiomyopathy

As listed by the trial registrant

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