By European Medicines Agency
Mylan N.V. and Biocon announced that the European Medicines Agency has accepted for review Mylan's Marketing Authorisation Application for a proposed biosimilar Trastuzumab, which is used to treat certain HER-2 positive breast and gastric cancers. This is the second biosimilar submission developed by the partnership that has been accepted for review in Europe.Powered by Capital Market - Live News
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