FDAnews
www.fdanews.com/articles/11296-eu-expands-ce-mark-for-dako-companion-diagnostics

EU Expands CE Mark for Dako Companion Diagnostics

February 24, 2017

Agilent Technologies has receive an expanded CE mark for its Dako PD-L1 IHC 22C3 pharmDx which can now be used to determine PD-L1 expression status to inform the first-line treatment of metastatic non-small cell lung cancer patients with Keytruda.

The intended use allows PD-L1 IHC 22C3 pharmDx to detect PD-L1 expression in both untreated and previously treated metastatic patients.