Bristol Myers (BMY) Gets FDA Approval for CAR T-Cell Therapy

 | Feb 09, 2021 07:24AM ET

Bristol Myers (NYSE:BMY) Squibb BMY announced that the FDA has approved its CD19-directed chimeric antigen receptor (CAR) T cell therapy, Breyanzi (lisocabtagene maraleucel; liso-cel).

The therapy is approved for the treatment of adult patients with relapsed or refractory (R/R) large B-cell lymphoma (LBCL) after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified (including DLBCL arising from indolent lymphoma), high-grade B-cell lymphoma, primary mediastinal large B-cell lymphoma and follicular lymphoma grade 3B.

This new promising immunotherapy involves using a patient’s own immune cells to attack cancer cells. The candidate was added to the company’s portfolio with the acquisition of Celgene Corporation (NASDAQ:CELG).

The FDA approval of Breyanzi was based on data from the TRANSCEND NHL 001 (017001) study, in which 268 patients with R/R LBCL received Breyanzi. In the study, the therapy demonstrated a 73% overall response rate and a 54% complete response (CR) rate. Breyanzi demonstrated sustained responses in patients who achieved a CR with a median duration of response not reached.

It has been granted the Priority Medicines (PRIME) designation for R/R DLBCL in the European Union and a Marketing Authorization Application (MAA) is currently under review with the European Medicines Agency.

While this innovative space promises potential, competition is stiff from the likes of Novartis’ GILD Yescarta.

Meanwhile, approval of new drugs will add a new stream of revenues for Bristol Myers, which should propel growth in the coming quarters.

The company’s shares have lost 9.2% in the past year against the industry 's growth of 14.1%.