New study tracks families with rare gene to unlock blood cancer secrets
NCT ID NCT07019155
First seen Nov 20, 2025 · Last updated Apr 29, 2026 · Updated 19 times
Summary
This study follows people with a gene change (DDX41) that raises the risk of blood cancers like MDS and AML, along with their relatives. Researchers will collect health information, blood, and other samples over 10 years to learn how these inherited risks lead to cancer. No treatments are tested—the goal is simply to observe and understand the disease process.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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