UK health technology assessor the National Institute for Health and Care Excellence (NICE) has issued a Final Appraisal Determination (FAD) recommending Opdivo (nivolumab) plus Yervoy (ipilimumab) for patients with previously untreated advanced renal cell carcinoma (RCC) that is intermediate- or poor-risk, US pharma major Bristol Myers Squibb (NYSE: BMY) has revealed.
In appraising the treatment, the NICE considered additional data collected since 2019 through the Cancer Drugs Fund, as well as data from the Checkmate-214 trial.
The decision is supported by five-year data from the Checkmate-214 trial, which showed improved overall survival (OS) and overall response rates (ORR) compared to sunitinib. The NICE decision means the combination will continue to be a treatment option for patients diagnosed with intermediate- or poor-risk advanced RCC in England.
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