FDA approves axicabtagene ciloleucel for second-line treatment of large B-cell lymphoma

FDA

1 April 2022 - Today, the Food and Drug Administration approved axicabtagene ciloleucel (Yescarta, Kite Pharma) for adult patients with large B-cell lymphoma 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.

Read FDA press release

Michael Wonder

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Michael Wonder

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Cancer , Outcome , US , Cellular therapy