European Commission approves Merck’s Keytruda (pembrolizumab) plus chemotherapy for new first-line indications in advanced HER2 negative gastric or GEJ adenocarcinoma in tumours expressing PD-L1 (CPS ≥1) and advanced biliary tract cancer

Merck/MSD

18 December 2023 - Keytruda now approved for 26 indications in the EU, including seven in gastro-intestinal cancers.

Merck today announced the European Commission has approved two new indications for Keytruda, Merck’s anti-PD-1 therapy, in two gastro-intestinal cancers.

Read Merck/MSD press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Cancer , Outcome , Medicine , Europe