Steven Powell, chief executive of UK-based immuno-oncology (I-O) company Macrophage Pharma, gives an overview of developments in this fast-moving space in an Expert View piece.
I-O has dominated the cancer therapy development landscape since the approval of Yervoy (ipilimumab: Bristol-Myers Squibb) in March 2011, followed by the antibody checkpoint inhibitors, Keytruda (pembrolizumab: Merck & Co) in September 2014 and Opdivo (nivolumab: B-MS) in December 2014.
These anti-CTLA-4 and anti-PD-1 checkpoint inhibitors have since been joined by the anti-PD-L1 agents Tecentriq (atezolizumab: Roche/Genentech); Imfinzi (durvalumab: AstraZeneca) and Bavencio (Merck KGaA/Pfizer).
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