17 December 2021 - If approved, PADCEV would be the first medicine for patients in the EU who have received prior platinum-based chemotherapy and a PD-1/L1 inhibitor.
Astellas Pharma and Seagen today announced that the CHMP of the EMA has adopted a positive opinion, recommending approval of the antibody-drug conjugate Padcev (enfortumab vedotin) as monotherapy for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received platinum-containing chemotherapy and a PD-1/L1 inhibitor.