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New registry aims to unlock secrets of rare cholesterol disease

NCT ID NCT01109368

First seen May 08, 2026 · Last updated May 22, 2026 · Updated 4 times

Summary

This study creates a registry for up to 60 children and adults in the U.S. with homozygous familial hypercholesterolemia (hoFH), a rare genetic condition causing extremely high cholesterol from birth. Researchers will track participants' overall health and cholesterol buildup in arteries over time, and collect blood samples to find new markers of artery disease. The goal is to better understand the disease and how it responds to treatments, helping design future studies.

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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

Study contacts

  • Contact

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

Locations

  • Weill Cornell Medical College

    RECRUITING

    New York, New York, 10021, United States

    Contact

    Contact

    Contact

    Contact

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

    Contact

    Contact

Conditions

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