Shares in New Jersey, USA-based Merck & Co (NYSE: MRK) gained 6% yesterday after the company announced its Phase III KEYNOTE-189 trial of Keytruda (pembrolizumab) met its co-primary endpoints, boosting confidence in its ability to lead in the market for first-line lung cancer therapies.
The trial is designed to compare a combination of the checkpoint inhibitor with Alimta (pemetrexed) and cisplatin or carboplatin, with Alimta and chemo alone, for the first-line treatment of patients with non-small cell lung cancer (NSCLC).
Roger Perlmutter, president of Merck’s research division said the study “showed significant improvement in overall survival and progression-free survival for patients receiving Keytruda.”
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 accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
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
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze