The hemophilia market is a challenging and competitive field but Sanofi is confident that fitusiran, which has just been given the green light by the US Food and Drug Administration (28 March), has the potential to change the disease landscape thanks to the therapy’s effective bleed protection, infrequent dosing and easy administration.
Key Takeaways
- Qfitlia approved as the first therapy in the US to treat hemophilia A or B with or without inhibitors
- The antithrombin-lowering subcutaneous...
The agency has approved fitusiran, which will be marketed as Qfitlia, as the first antithrombin (AT)-lowering therapy for routine prophylaxis to prevent or reduce the...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip 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?