At this year’s American Society of Clinical Oncology (ASCO) meeting, Bristol Myers Squibb (NYSE: BMY) will present the first data from a Phase III trial evaluating a LAG-3-blocking antibody.
The firm has already released top-line results from the RELATIVITY-047 trial, revealing a fixed-dose combination of LAG-3 blocker relatlimab and Opdivo (nivolumab) met its primary endpoint of progression-free survival (PFS), in the first-line treatment of melanoma.
Jonathan Cheng, senior vice president and head of oncology development, describes relatlimab as “a very exciting new area,” adding it is now “the third checkpoint inhibitor to show benefit in patients with melanoma.”
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