Swiss pharma giant Novartis (NOVN: VX) has entered into a voluntary licensing agreement for its chronic myeloid leukemia (CML) drug with the Medicines Patent Pool (MPP), agreeing to the production of generics in low-and-middle income countries.
The MPP announced on the side-lines of the World Cancer Congress that the accord would increase access to nilotinib, a twice daily oral medicine used to treat CML, part of the World Health Organization Model List of Essential Medicines (WHO EML), for the treatment in adults and children of at least one year of age.
Marketed as Tasigna, the drug generated sales of $2.1 billion for Novartis last 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