Bristol-Myers Squibb's (BMY) Abecma Approved in EU

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Bristol Myers Squibb’s Abecma (idecabtagene vicleucel) Becomes First CAR T Cell Therapy Approved in the European Union in Earlier Lines for Triple-Class Exposed Relapsed and Refractory Multiple Myel

March 20, 2024 4:45 PM EDT

Abecma demonstrated superiority over standard regimens in the Phase 3 KarMMa-3 trial, with a 51% reduction in risk of disease progression or death and a well-established safety profile with mostly low-grade and transient occurrences of cytokine release syndrome and neurotoxicity

Approval reinforces Bristol Myers Squibbs commitment to bring the transformative potential of cell therapy into earlier lines of treatment

PRINCETON N.J.--(BUSINESS... More