New repository aims to unlock secrets of rare, deadly cholesterol disease

NCT ID NCT01109368

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study creates a database of health information and blood samples from up to 60 children and adults with homozygous familial hypercholesterolemia (hoFH), a rare genetic condition causing extremely high cholesterol from birth. Researchers will track participants over time to learn how the disease progresses and how different treatments affect cholesterol buildup in arteries. The goal is to improve future care and help design better clinical trials for this life-threatening disorder.

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 repository could help researchers develop better treatments and monitoring strategies for people with this rare, severe cholesterol disorder.

What could go wrong

This is an observational study, not a treatment trial. It will not directly improve health for participants, and results may take years to influence care.

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.

homozygous familial hypercholesterolemia

As listed by the trial registrant

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

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

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