The publication of a second draft recommendation not recommending use of Takeda Pharmaceutical’s (TYO: 4502) Adcetris (brentuximab vedotin) in relapsed or refractory Hodgkin lymphoma (R/R HL) on the UK's National Health Service (NHS), has prompted fresh criticism from the Japanese drugmaker.
The drug is the current standard of care in this indication and it will remain so under the Cancer Drugs Fund (CDF) until the culmination of this review by the National Institute for Health and Care Excellence (NICE), the cost-effectiveness watchdog for England and Wales. The final decision is expected in March 2017.
"The clinical community is on the brink of losing a medicine that is the standard of care"
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