Agilent (A) Gets FDA Approval For Cervical Cancer Test Assay

 | Jun 13, 2018 10:03PM ET

Agilent Technologies (NYSE:A) recently received approval from the FDA for a cervical cancer diagnostic assay, named PD-L1 IHC 22C3 pharmDx, for expanded use.

Following the FDA approval, PD-L1 IHC 22C3 pharmDx became the first IHC test for determining PD-L1 expression in cervical cancer. Also, it is now the first FDA-approved companion diagnostic to identify patients with cervical cancer for treatment with KEYTRUDA.

KEYTRUDA is an anti-PD-1 therapy manufactured by Merck (NYSE:MRK) & Co. MRK.

This new step facilitates the company to expand in the growing cancer-diagnostic market.

Coming to share price, Agilent has underperformed its industry on a year-to-date basis. The stock has registered a loss of 11.59% against the industry ’s growth of 13.47%.