European Commission decision supports Biogen's pursuit of market exclusivity
The European Commission (EC) has withdrawn its marketing authorizations for generic versions of Tecfidera (dimethyl fumarate), an oral therapy approved in Europe for relapsing-remitting multiple sclerosis (RRMS).
I personaly think it has do with money and control. But this is what the website says:
According to Biogen, which developed and markets the brand-name medication, the decision ensures Biogen will have full data and marketing protection for Tecfidera at least until Feb. 3, 2025. That means it will be the sole dimethyl fumarate MS therapy that may be marketed for sale legally in the European Union.
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