Samsung Bioepis has told Generics Bulletin that is it is “not in position to specify at this time” when it will launch its biosimilar to AstraZeneca’s Soliris (eculizumab) treatment of adult and child paroxysmal nocturnal hemoglobinuria (PNH), after the European Commission approved the Korean firm’s product – the second to receive approval in the EU.
In late March, Samsung Bioepis followed Amgen in obtaining a positive opinion recommending granting a pan-European marketing authorization for a biosimilar to Soliris,
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Generics Bulletin for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?