Scientists hunt for genetic clues in rare blood disorders
NCT ID NCT05028621
First seen Feb 23, 2026 · Last updated May 14, 2026 · Updated 10 times
Summary
This study looks at the DNA of people with rare blood diseases like Castleman disease and histiocytosis. The goal is to find genetic changes that could be targeted with existing or new treatments. About 135 participants will provide samples for genetic testing. The study is currently on hold.
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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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Cleveland Clinic, Case Comprehensive Cancer Center
Cleveland, Ohio, 44106-5065, United States
Conditions
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