EMA validates application for CAR-T cell therapy Breyanzi from BMS – The Pharma Letter

The European Medicines Agency (EMA) has validated the type II variation application for extension of the indication for Breyanzi (lisocabtagene maraleucel) to treat adult patients with diffuse large B-cell lymphoma (DLBCL), high grade B-cell lymphoma (HGBCL), primary mediastinal large B-cell lymphoma (PMBCL) and follicular lymphoma grade 3B (FL3B), who are refractory or have relapsed within 12 months of initial therapy and are candidates for hematopoietic

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EMA validates application for CAR-T cell therapy Breyanzi from BMS - The Pharma Letter