US FDA calls for USFDA boxed warning changes on CAR-T cancer therapies
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London: The U.S. Food and Drug Administration said on Thursday cancer therapies that use CAR-T technology will require changes to the so-called ''boxed warning'' to highlight the serious risk of T-cell blood cancer in patients who use these therapies.
The health regulor has required related updates to other sections of the label such as warnings and precautions, postmarketing experience, patient counseling information and medication guide.
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