BMS’ Breyanzi (lisocabtagene maraleucel) Receives the US FDA’s Approval for Adults With R/R Large-B-Cell Lymphoma

February 8, 2021 Auto Bot Adults, FDA, regulatory 0

Shots:

  • The approval is based on pivotal TRANSCEND NHL 001 (017001) study assessing Breyanzi in 268 patients with 3L+R/R LBCL including patients with a broad range of histologies and high-risk disease. Breyanzi was administered in the inpatient & outpatient settings
  • Results: ORR (73%); CR (54%); PR (19%); mDOR (16.7mos.) in all responders; patients with best response or PR, mDOR (1.4mos.); patients achieving CR, 65% had remission lasting at least 6mos. and 62% had remission lasting at least 9mos.
  • Breyanzi is a CD19-directed CAR T cell therapy with defined composition and 4-1BB costimulatory domain. Additionally, the US FDA has granted ODD, RMAT and BT Designation to the therapy

Click here, Click here ­to­ read full press release/ article | Ref: PRNewswire, BMS | Image: PRNewswire, BMS

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