Janssen Pharmaceutical Cos. and Legend Biotech Corp. are seeing similar response rates for their BCMA-targeting CAR-T therapy ciltacabtagene autoleucel (cilta-cel) in earlier multiple myeloma settings. The partners presented data at the American Society of Hematology (ASH) meeting that show response rates in multiple myeloma patients in the second through fourth lines of treatment that match the high and long-lasting responses seen in patients with much more advanced forms of the disease.
The data were revealed on 12 and 13 December, almost six weeks after Janssen, a Johnson & Johnson subsidiary, and Legend announced a three-month delay in the US Food and Drug Administration approval decision for cilta-cel in relapsed or refractory multiple myeloma, moving the action date from 28 November to 28 February. The shift gave Abecma (idecabtagene vicleucel) from Bristol Myers Squibb Company and 2seventy Bio, Inc