The European Medicines Agency’s advisory group CHMP has adopted a positive opinion recommending approval of the combination of Merck’s (NYSE:MRK) Keytruda (pembrolizumab) and Pfizer’s (NYSE:PFE) Inlyta (axitinib) for the first-treatment of advanced renal cell carcinoma.
A final decision from the European Commission usually takes ~60 days.
MRK is up 1% premarket. This morning is also announced positive data from a late-stage study of Keytruda in triple-negative breast cancer.
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