New hope for families cursed by inherited cancer gene

NCT ID NCT07524530

Summary

This study is testing a personalized stem cell transplant for people with blood cancers caused by an inherited mutation in the RUNX1 gene. Researchers will tailor the doses of chemotherapy and other medications to each patient, aiming to improve survival rates compared to standard transplants. The study will enroll up to 98 participants, including patients, their family members, and healthy volunteers.

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: •••••@•••••

  • Contact

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

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

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

Conditions

Explore the condition pages connected to this study.