Efficacy: (n = 74; 2L+); dose: either 50 x 106 or 100 x 106 CAR-positive viable T cells
median follow-up: 16.1 months
ORR: 86.5%
CR: 74.3%
Safety: (n = 88)
Breyanzi was well-tolerated and no new safety signals were observed
Any grade CRS: 61%; Grade 3/4 CRS: 1%; no Grade 5 CRS reported
Any grade Nes: 31%; Grade 3/4 NEs: 9%; no Grade 5 NEs reported
“Based on results from TRANSCEND FL and TRANSCEND NHL 001, Breyanzi continues to demonstrate the ability to elicit significant deep and durable responses alongside a manageable safety profile, potentially addressing areas of high unmet need and reinforcing our commitment to advancing innovative solutions for the broadest array of hematologic malignancies of any CD19-directed CAR T cell therapy.” said Anne Kerber, senior vice president, head of Cell Therapy Development, Bristol Myers Squibb