By Matt Grossman
Roche Holding AG has gained approval from the U.S. Food and Drug Administration for a diagnostic test used to determine whether patients with endometrial cancer will benefit from a particular treatment.
The test, called Ventana MMR RxDx, can help physicians decide whether an endometrial cancer patient should be treated with Jemperli, an anti-PD1 immunotherapy from GlaxoSmithKline PLC.
The test uses a comprehensive panel of DNA mismatch repair biomarkers tested by immunohistochemistry, Roche said.
Write to Matt Grossman at matt.grossman@wsj.com
(END) Dow Jones Newswires
04-23-21 0632ET