Eli Lilly (NYSE: LLY) has announced top-line results from its Phase III REACH-2 study of Cyramza (ramucirumab) as a second-line treatment for liver cancer patients.
The trial met its primary endpoint of overall survival (OS) as well as the secondary endpoint of progression-free survival (PFS). The efficacy and safety results will be submitted for presentation at a future medical meeting.
The firm says the safety profile in the study was consistent with what has been previously observed for single-agent Cyramza, and that it intends to initiate regulatory submissions in mid-2018.
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