May is something of a key month for Eylea (aflibercept), one of the largest biosimilar opportunities set to materialize in the current decade. Its US market exclusivity will officially run its course on 17 May, allowing the US Food and Drug Administration to begin approving biosimilars to the multi-billion-dollar treatment for neovascular age-related macular degeneration and diabetic macular edema.
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?