31 January 2025 - Recommendation based on the Phase 2 TRANSCEND FL study in which 97.1% of patients responded to Breyanzi, with 94.2% of patients achieving complete response.
Bristol Myers Squibb today announced the CHMP of the EMA has recommended approval of Breyanzi (lisocabtagene maraleucel; liso-cel), a CD19 directed chimeric antigen receptor T cell therapy, for the treatment of adult patients with relapsed or refractory follicular lymphoma who have received two or more prior lines of systemic therapy.