
Independent French pharma major Servier announced that the UK’s National Institute for Health and Care Excellence (NICE) has published final draft guidance recommending Voranigo (vorasidenib), a once-daily oral targeted therapy indicated for the treatment of Grade 2 astrocytoma or oligodendroglioma with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation or isocitrate dehydrogenase-2 (IDH2) mutation in adults and pediatric patients 12 years and older, who are not in need of immediate chemotherapy or radiotherapy following surgical intervention.
Based on NICE’s final draft guidance published on March 31, recommending vorasidenib, immediate access is available to eligible patients across England and Wales via interim funding through the cancer drugs fund (CDF).
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
| Headless Content Management with Blaze