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USFDA approves Breyanzi, new CAR T Cell therapy for adults
Global biopharmaceutical company Bristol Myers Squibb (BMS) has received US Food and Drug Administration (USFDA) approval for its new CD19-directed chimeric antigen receptor (CAR) T cell therapy Breyanzi (lisocabtagene maraleucel; liso-cel).
United states
Meghan gutierrez
Samit hirawat
Bristol myers squibb
European union
European medicines agency
Drug administration
Lymphoma research foundation
Myers squibb
Risk evaluation
Mitigation strategy
Cell therapy
Research foundation
Breyanzi priority medicines
Marketing authorization application
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