By Ben Glickman


Bristol Myers Squibb's blood cancer treatment has received approval from European regulators in certain cases.

The pharmaceutical company said Wednesday that Abecma, an immunotherapy, has been approved by the European Commission for treating adults with relapsed and refractory multiple myeloma who have received at least two prior therapies.

Bristol Myers Squibb said Abecma has kept its Orphan Designation for the treatment of multiple myeloma in the European Union.

Abecma last week was determined by a U.S. Food and Drug Administration advisory committee to have a favorable risk-benefit profile in triple-class exposed relapsed or refractory forms of multiple myeloma.

The treatment is being jointly developed and commercialized in the U.S. with 2seventy Bio.


Write to Ben Glickman at ben.glickman@wsj.com


(END) Dow Jones Newswires

03-20-24 1737ET