Experimental stem cell transplant could reduce toxic side effects for fanconi anemia patients
NCT ID NCT04784052
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new way to treat Fanconi Anemia, a rare genetic disorder that causes bone marrow failure. Doctors will give patients donor stem cells that have been specially filtered to remove certain immune cells, along with an experimental antibody called JSP191. The goal is to help the new cells grow and rebuild the blood system with fewer severe side effects than standard chemotherapy. The trial is recruiting 18 participants and will follow them for up to 2 years after the transplant.
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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.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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Locations
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Stanford University
RECRUITINGStanford, California, 94305, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••