The German Institute for Quality and Efficiency in Health Care (IQWiG) examined in a dossier assessment whether ceritinib offers an added benefit over the appropriate comparator therapy. Such an added benefit cannot be derived from the dossier, however, because it contained no data suitable for the assessment, the medicines watchdog body said.
Zykadia (ceritinib) from Swiss pharma giant Novartis (NOVN: VX) received European Commission approval earlier this year to treat adult patients with anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC) previously treated with crizotinib(The Pharma Letter May 8).
The Federal Joint Committee (G-BA) distinguished between two research questions: In patients who are eligible for chemotherapy with docetaxel or pemetrexed, ceritinib was to be compared with one of these two drugs.
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