Biotie Closes Eventful Year with A European Filing of Nalmefene
Biotie Therapies Oyj closed out the year exactly as planned – with a product undergoing regulatory review in Europe. Development partner H. Lundbeck A/S disclosed on Dec. 21 that the European Medicines Agency (EMA) had accepted for review its marketing authorization application (MAA) for nalmefene to treat alcohol dependence.
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