CRISPR gene editing trial seeks to reboot immune system against incurable blood cancer
NCT ID NCT07340853
Summary
This early-stage trial is testing a new treatment for multiple myeloma that has returned or stopped responding to standard therapies. Doctors will collect patients' own immune cells, use CRISPR gene-editing technology to reprogram them to attack cancer, then infuse them back into the body. The study aims to find the safest and most effective dose for 30 adults with advanced disease.
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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