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FDA panel recommends approval for gene-altering leukemia treatment

By The New York Times  
   July 13, 2017

A Food and Drug Administration panel opened a new era in medicine Wednesday, unanimously recommending that the agency approve the first treatment that genetically alters a patient's own cells to fight leukemia, transforming them into what scientists call "a living drug" that powerfully bolsters the immune system to shut down the disease.

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