NYSE:ALife Sciences
Agilent’s New FDA Approval And What It Could Mean For Investors
Agilent Technologies (NYSE:A) received FDA approval for its PD-L1 IHC 22C3 pharmDx as the only authorized companion diagnostic for certain ovarian and related cancers treated with KEYTRUDA.
The approval covers use of the assay to help identify patients who may be eligible for KEYTRUDA based on PD-L1 expression.
The decision expands the clinical indications for PD-L1 IHC 22C3 pharmDx within Agilent's broader oncology diagnostics portfolio.
For investors, this news sits at the intersection of...