Chinese biotech BeiGene (Nasdaq: BGNE) has announced that the global Phase III RATIONALE 301 trial with tislelizumab met its primary endpoint of non-inferior overall survival (OS) versus sorafenib as a first-line treatment in adults with unresectable hepatocellular carcinoma (HCC).
Sorafenib, which was co-developed and co-marketed by Bayer (BAYN: DE) and Onyx Pharmaceuticals as Nexavar, is a kinase inhibitor that has been on the market in the USA and Europe for HCC, the most common form of liver cancer, for nearly 15 years.
There were no alarms on the safety front in the RATIONALE trial, which involved more than 600 patients in the USA, Europe, and Asia.
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