U.S. FDA approves new label update for CAR T-cell therapy Yescarta showing prophylactic steroid use improves management of cytokine release syndrome

Gilead

31 January 2022 - Updated toxicity management strategy can improve certain adverse events without compromising the activity of Yescarta.

Kite today announced the U.S. FDA has approved an update to the prescribing information for Yescarta (axicabtagene ciloleucel) to include use of prophylactic corticosteroids across all approved indications. 

Yescarta is now the first and only chimeric antigen receptor (CAR) T-cell therapy with information in the label to help physicians manage, and potentially prevent, treatment side effects.

Read Gilead press release

Michael Wonder

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Michael Wonder

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Outcome , US , Cellular therapy