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ImmunityBio announces Anktiva MAA accepted for review by EMA

ImmunityBio (IBRX) announced the European Medicines Agency has accepted for review and begun assessing the marketing authorization application for Anktiva in combination with Bacillus Calmette-Guerin for the treatment of patients with BCG-unresponsive non-muscle invasive bladder cancer with carcinoma in situ, with or without papillary tumors. The EMA covers 27 countries in the European Union, as well as Iceland, Norway and Liechtenstein.

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