US FDA approval of Sanofi/Regeneron Pharmaceuticals Inc's PD-1 inhibitor Libtayo (cemiplimab-rwlc) in a niche market for cutaneous squamous cell carcinoma (CSCC) paves the way for development across a range of other indications as well for the partners' immuno-oncology strategy more generally.
FDA approved Libtayo on Sept. 28 for locally advanced squamous cell carcinoma (CSCC) in patients who are not candidates fur curative surgery or radiation and metastatic CSCC, ahead of 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?