US clears first ‘living drug’ for tough childhood leukemia

WASHINGTON (AP) — The Food and Drug Administration has approved the first treatment that genetically engineers patients’ own blood cells to seek and destroy childhood leukemia. The move opens a new era in cancer care.

FDA’s action Wednesday makes Novartis Pharmaceutical’s CAR-T cell treatment the first type of gene therapy to hit the U.S. market. It’s one in a wave of “living drugs” being developed for blood cancers and maybe other tumors, too.

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Full story from AP on WOODTV.com


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