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

Last Updated: Tuesday, April 12, 2022

Based on data from the randomized, open-label, multicenter ZUMA-7 trial, the FDA approved the use of anti-CD19 CAR T-cell therapy axicabtagene ciloleucel in adult patients with large B-cell lymphoma refractory to first-line chemoimmunotherapy or that relapses within 12 months of first-line chemoimmunotherapy.

U.S. Food and Drug Administration
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