The European Medicines Agency’s advisory group CHMP has adopted a positive opinion backing approval of Bristol-Myers Squibb’s (NYSE:BMY) Empliciti (elotuzumab) plus Celgene’s (NASDAQ:CELG) Pomalyst (pomalidomide) and low-dose dexamethasone for the treatment of adults patients with relapsed/refractory multiple myeloma who have received at least two prior lines of therapy, including Celgene’s Revlimid (lenalidomide) and a protease inhibitor, and have experienced cancer progression on the last therapy.
A final decision from the European Commission usually takes ~60 days.
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