Patients have been dealt a major blow after the first ever treatment for AL amyloidosis, a rare incurable condition, was rejected by the UK’s National Institute for Health and Care Excellence (NICE).
Darzalex Faspro (the subcutaneous formulation of daratumumab), in combination with bortezomib, cyclophosphamide and dexamethasone (VCd or CyBorD in short), is marketed for the treatment of newly-diagnosed light chain (AL) amyloidosis by Janssen, the pharmaceutical arm of US healthcare giant Johnson & Johnson (NYSE: JNJ). All four drugs are already individually available on the National Health Service (NHS).
Up to 600 patients would have benefitted from the life-extending treatment, known as Dara-CyBorD, each year. The news comes three months after the same treatment was approved and rolled out to newly-diagnosed patients in Scotland on the (NHS). 0
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