In a U-turn by the UK drug watchdog, in its latest appraisal, the National Institute for Health and Clinical Excellence (NICE) has reversed its draft guidance and approved the use of Mepact (mifamurtide), from Japan’s largest drugmaker Takeda (TYO: 4502), for high grade non-metastatic osteosarcoma in children, adolescents and young adults aged between two and 30 (The Pharma Letter October 8, 2010).
The NICE Board has clarified how discounting is applied to its “methods guide” and, Takeda explained, this considers the cost effectiveness of a treatment when both discounting of costs and health effects is applied.
Discount clarification plus new PAS reduces QALY
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