Radicava (edaravone), an intravenous therapy indicated for all adult patients diagnosed with amyotrophic lateral sclerosis (ALS) from Japanese drugmaker Mitsubishi Tanabe Pharma (TYO: 4508), is now available in the USA.
It is the first US Food and Drug Administration-approved treatment in 22 years for ALS, an incurable neurodegenerative condition also known as Lou Gehrig’s disease, that affects the nerve cells in the brain and spinal cord.
Atsushi Fujimoto, president of Mitsubishi Tanabe Pharma America, said: “It gives me great joy that Radicava is now available in the USA.
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