The European Medicines Agency’s human medicines committee (CHMP) recommended seven novel medicines for approval at its June 2022 meeting, including the first gene therapy for hemophilia A.
The committee adopted a positive opinion for Pepaxti (melphalan flufenamide), from Swedish biotech Oncopeptides (Nasdaq Stockholm: ONCO), for the treatment of multiple myeloma, a rare cancer of the bone marrow that affects plasma cells, a type of white blood cell that produces antibodies.
US pharma major Eli Lilly’s (NYSE: LLY) Rayvow (lasmiditan), intended for the treatment of migraine in adults, received a positive opinion from the CHMP. It is estimated that approximately 15% of the EU population suffers from migraine, according to the EMA.
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