Gene-Edited immune cells take on Hard-to-Treat myeloma
NCT ID NCT07340853
First seen Jan 24, 2026 · Last updated May 21, 2026 · Updated 19 times
Summary
This early-phase trial tests a new treatment for multiple myeloma that has come back or stopped responding to standard therapies. The treatment uses a patient's own immune cells, modified in the lab with CRISPR gene editing to target and attack cancer cells. About 30 adults will receive the cells after a short chemotherapy course, with the main goals being safety and finding the best dose.
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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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University of California, San Francisco
RECRUITINGSan Francisco, California, 94143, United States
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