U.S. FDA approves multiple myeloma therapy

News

Date: 31.03.2021

The U.S. Food and Drug Administration has approved Bristol-Myers Squibb Co and bluebird bio Inc’s multiple myeloma therapy, ide-cel, acquired as part of its $74 billion buyout of Celgene, the drugmakers said in a joint statement late on Friday.

Ide-cel is a CAR-T therapy that involves taking immune cells from a patient, engineering them to attack tumor cells and infusing them back into the patient.

Bristol Myers Squibb and partner bluebird bio Last year resubmitted its application for ide-cel after the U.S. drug regulator declined to review the treatment and sought more information.

As part of the Celgene-Bristol Myers deal, Celgene shareholders would have received a $9 per share payment if three of Celgene’s top pipeline assets were approved by certain dates.

However, the FDA did not approve blood cancer therapy, liso-cel, by the end of 2020 and as a result the CVR agreement was terminated.

The article was prepared based on the information: Reauters

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