Bristol-Myers Squibb and AbbVie receive U.S. FDA Breakthrough Therapy Designation for Elotuzumab, an investigational humanized monoclonal antibody for multiple myeloma
20 May 2014 | By Bristol-Myers Squibb
Bristol-Myers Squibb Company and AbbVie announced that the U.S. Food and Drug Administration has granted elotuzumab, an investigational humanized monoclonal antibody, Breakthrough Therapy Designation for use in combination with lenalidomide and dexamethasone...