Aurobindo is gearing up to make its first immunology biosimilar filing in FY24/25, with regulatory approval likely to open the gateway to a $4bn opportunity for the drug in markets like Europe and US should it be among the first three companies to launch.
So far, it has filed applications for two oncology biosimilars in the EU via its subsidiary CuraTeQ Biologics Private Ltd
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?