Funding cetuximab for patients with head and neck cancer will be a significant advance for treating this type of cancer in New Zealand, says Sarah Fitt, director of operations at the Pharmaceutical Management Agency PHARMAC.
Marketed in New Zealand by Merck Serono Australia, a subsidiary of Germany’s Merck KGaA (MRK: DE), as Erbitux, cetuximab will be available from February 1, 2018 as an additional treatment option for people with locally advanced, non-metastatic head and neck cancer who are unable to use the current standard chemotherapy treatment, cisplatin.
Cetuximab is an infusion given in tandem with radiation therapy. PHARMAC expects that 40-50 people will be eligible for treatment every year.
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