Biocon Biologics’ receives FDA approval for Biosimilar Aflibercept for Yesafili
The approval of YESAFILI marks Biocon Biologics’ expansion into the ophthalmology therapeutic area in the United States
The approval of YESAFILI marks Biocon Biologics’ expansion into the ophthalmology therapeutic area in the United States
This agreement paves the way for the introduction of YESAFILI into the Canadian market
Yesafili, received marketing authorization approval from the European Commission for the European Union
We are redesigning Bayer to focus only on what’s essential for our mission, ‘Health for all, hunger for none’”
The centralized marketing authorization granted by the EC is valid in all EU Member States as well as in the European Economic Area (EEA) countries Iceland, Liechtenstein and Norway
Lupin’s subsidiary in Philippines, Multicare Pharmaceuticals, will file for marketing approval and be responsible for distribution and commercialization of the biosimilars once approved.
Company's net income rose by 57.5 percent to 3.291 billion euros in Q1
Aflibercept is the second biosimilar product that has entered the clinical trial phase after biosimilar Adalimumab
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