UK medicines cost-effectiveness watchdog the National Institute for Health and Care Excellence (NICE) has recommended US pharma major AbbVie’ (NYSE: ABBV) Humira(adalimumab) for the treatment of active moderate to severe hidradenitis suppurativa (HS) in adult patients with an inadequate response to conventional systemic HS therapy, as per the marketing authorization for adalimumab.
This is a change in position following draft guidance in which the NICE Appraisal Committee was minded not to recommend adalimumab and requested further analyses from the company. Following this latest recommendation, suitable patients in England and Wales should be able to access adalimumab on the National Health Service.
Humira is AbbVie’s mega-blockbuster arthritis drug, which has a range of additional indications in other inflammatory conditions and generated sales of over $14 billion in 2015.
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