Amgen Announces EU Approval for Vectibix
Amgen announced that the European Commission has approved to extend the therapeutic indications for Vectibix, a therapy to treat colorectal cancer.
US-based biotechnology company Amgen announced Tuesday that the European Commission has approved a variation to the marketing authorization for Vectibix? (panitumumab) to include indications for the treatment of patients with wild-type KRAS metastatic colorectal cancer (mCRC) in first-line in combination with FOLFOX and in second-line in combination with FOLFIRI in patients who have received first-line fluoropyrimidine-based chemotherapy (excluding irinotecan).
This approval of Vectibix applies to all 27 European Union (EU) member states. Prior to this approval, Vectibix had received conditional approval in the EU as monotherapy. The monotherapy indication was also further revised to state that Vectibix is indicated for the treatment of patients with wild-type KRAS mCRC as monotherapy after failure of fluoropyrimidine-, oxaliplatin-, and irinotecan
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