Regulators in the US have followed their counterparts in Europe by giving the green light to Pfizer Inc.'s rare blood cancer drug Besponsa, although the approval comes with a boxed warning which could dampen the targeted therapy's sales potential.
Besponsa (inotuzumab ozogamicin) has been approved by the US Food and Drug Administration as a treatment for relapsed or refractory...
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?