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Merck has announced today that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion recommending approval of KEYTRUDA® (pembrolizumab).
Pivotal Phase 3 data demonstrated potential of Tildrakizumab to offer patients treatment for moderate-to-severe plaque psoriasis without burden of frequent injections
UK-based biopharmaceutical company Mereo BioPharma has announced that its BPS-804 drug has been accepted to participate in the European Medicines Agency’s (EMA) adaptive pathways programme.
The European Commission (EC) has ratified positive opinion for the annual renewal of PTC Therapeutics’ Translarna (ataluren) marketing authorisation for the treatment of nonsense mutation duchenne muscular dystrophy (nmDMD).