Merck & Co adds more Ph III data for Keytruda in stomach cancer

19 June 2023
keytruda_big

Leading checkpoint blocker Keytruda (pembrolizumab) now has more than 30 approvals under its belt, and shows no sign of stopping, with new positive Phase III data in a rare cancer.

Merck & Co (NYSE: MRK) has unveiled results showing one of the co-primary endpoints has been met in the KEYNOTE-811 trial, with a statistically-significant outcome in progression-free survival (PFS).

The study is testing Keytruda, together with trastuzumab and chemotherapy, for people with (HER2)-positive advanced gastric or gastroesophageal junction (GEJ) adenocarcinoma.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biotechnology