Roche (ROG: SIX) has been granted US Food and Drug Administration approval for a combination of Tecentriq (atezolizumab) and Avastin (bevacizumab), plus chemo, for first-line treatment of metastatic non-squamous non-small cell lung cancer (NSCLC).
The approval, which was based on data from the Phase III IMpower150 study, applies to people with no EGFR or ALK genomic tumor aberrations.
The study showed that the triple combo helped people live significantly longer, compared to Avastin and chemotherapy alone, with median overall survival of 19.2 versus 14.7 months.
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