EU Authorizes Perioperative Pembrolizumab Plus Enfortumab Vedotin

Company Merck; Pfizer; Astellas Event Type Regulatory (European Commission Authorization) Modality Anti-PD-1 antibody plus Nectin-4 antibody-drug conjugate Asset Pembrolizumab (Keytruda) plus enfortumab vedotin (Padcev) Target PD-1; Nectin-4 Disease Area Resectable muscle-invasive bladder cancer (perioperative, cisplatin-eligible) Summary The European Commission authorized pembrolizumab plus enfortumab vedotin before…

🔒

Continue reading this signal

Create a free InSilens account to unlock full articles, analysis, and deal context.

Create Free Account
Share this article :

Leave a Reply

Your email address will not be published. Required fields are marked *