The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has issued positive opinions recommending marketing authorization for three of US drugmaker The Medicines Company’s (Nasdaq: MDCO) development candidates – Kengrexal (cangrelor), Orbactiv (oritavancin) and Raplixa (sealant powder).
Kengrexal is the first intravenous antiplatelet agent that provides immediate, consistent, and rapidly reversible P2Y12 inhibition; Orbactiv is the first single-dose intravenous antibiotic for treatment of acute bacterial skin and skin structure infections (ABSSSIs) caused by susceptible designated Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA); and Raplixa is the first ready-to-use, biologically active, powdered fibrin sealant that provides hemostasis in a wide range of bleeding settings. The recommendations were supported by Phase III results.
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