The National Institute for Health and Clinical Excellence (NICE), the medicines watchdog for England and Wales, has recommended Stelara (ustekinumab) in its definitive Technology Appraisal Guidance (TAG).
Stelara, marketed by Janssen, a subsidiary of US health care giant Johnson & Johnson (JNJ), is recommend as a treatment option for patients with active psoriatic arthritis, when the response to previous non-biological disease-modifying anti-rheumatic drug (DMARD) therapy has been inadequate. The drug generated sales of $2.07 billion, up 37.8% year on year, in 2014 for J&J.
In May 2014, the NICE issued technology appraisal guidance 313 which did not recommend using ustekinumab alone or in combination with methotrexate, for treating active psoriatic arthritis in adults when the response to previous non-biological DMARD therapy has been inadequate.
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