Moderna (Nasdaq: MRNA) and Merck & Co (NYSE: MRK) have announced that mRNA-4157/V940 alongside Keytruda (pembrolizumab) has been granted Priority Medicines (PRIME) scheme designation by the European Medicines Agency (EMA) for the adjuvant treatment of high-risk stage III/IV melanoma following complete resection.
mRNA-4157/V940 is an investigational personalized mRNA cancer vaccine while Keytruda is Merck's big-selling anti-PD-1 therapy.
The EMA granted PRIME scheme designation based on positive data from the Phase IIb KEYNOTE-942/mRNA-4157-P201 trial, results from which are due to be published later this month.
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