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FDA approves YESCARTA® (axicabtagene ciloleucel) for an additional indication.

04 Apr 2022 7:25 AM | Katy Monaco (Administrator)

Food and Drug Administration approved axicabtagene ciloleucel (Yescarta, Kite Pharma, Inc.) for adult patients with large B-cell lymphoma (LBCL) that is refractory to first-line chemoimmunotherapy or relapses within 12 months of first-line chemoimmunotherapy. It is not indicated for the treatment of patients with primary central nervous system lymphoma. More Information. Please see full Prescribing Information.

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