European Commission Approves Subcutaneous Administration of KEYTRUDA® (pembrolizumab) for All Adult Indications Approved in the European Union

Core Points - The European Commission has approved a new subcutaneous administration route and a new pharmaceutical form of KEYTRUDA, Merck's anti-PD-1 therapy [1] Company Summary - Merck, known as MSD outside the U.S. and Canada, will market the new formulation as KEYTRUDA SC in the European Union [1] - In the U.S., the product will be marketed as KEYTRUDA QLEX, which combines pembrolizumab and berahyaluronidase alfa-pmph [1]