Rare childhood blood cancers under the microscope: new registry aims to unlock secrets
NCT ID NCT07410247
First seen Feb 20, 2026 · Last updated May 23, 2026 · Updated 12 times
Summary
This study is creating a nationwide registry and biobank for children and teens diagnosed with rare blood cancers called myeloproliferative neoplasms (MPNs). The goal is to collect medical data and blood samples from 500 participants to better understand how these diseases behave in young people. This information will help doctors improve diagnosis and treatment tailored specifically for children.
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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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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Department of Pediatrics and Adolescent Medicine, University Hospital Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, Erlangen, Germany
RECRUITINGErlangen, Bavaria, D-91054, Germany
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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