In the first two months of 2018, seven products containing a new active substance received marketing authorizations through the EU's centralized procedure, including two treatments for hemophilia, new drugs for multiple sclerosis and diabetes, and two medicines for rare diseases – one for X-linked hyperphosphatemia, the other for preventing cytomegalovirus reactivation.
The two hemophilia drugs given the green light by the European Commission are Roche/Chugai's Hemlibra (emicizumab) and Shire's Adynovi (rurioctocog...






