US biotech major Biogen Idec’s (Nasdaq: BIIB) Indian subsidiary has received approval of the first oral therapy for multiple sclerosis, Tecfidera (dimethyl fumarate), from the Drug Controller General of India (DCGI), for people with relapsing-remitting multiple sclerosis (RRMS).
The new drug, which is already approved in the USA, Europe and other countries, will be available in the Indian market, commencing the second week of February 2015, said Biogen Idec India. For full-year 2014, Tecfidera revenues were $2.9 billion (compared with $876.1 million in 2013) consisting of $2.4 billion in US sales and $483 million in sales outside the USA.
First oral drug for RRMS cleared for marketing in India
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