Stada and Xbrane Biopharma have delivered on the promise of their proposed Lucentis (ranibizumab) biosimilar after their Ximluci version of the ophthalmology treatment received a positive opinion from the European Medicines Agency’s Committee for Medicinal Products for Human Use recommending granting a pan-European marketing authorization.
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?