Amgen wins race to gain EU approval for Humira biosimilar

24 March 2017
biosimilars_samples_large

As it did in the USA, biotech major Amgen (Nasdaq: AMGN) has become the first company to gain European Union (EU) approval for a biosimilar version of AbbVie's (NYSE: ABBV) Humira (adalimumab), the world’s best-selling branded drug.

The European Commission (EC) has granted marketing authorization for Amgen’s version of the anti-TNF-α monoclonal antibody, which it has branded Amgevita, in all available indications.

These indications cover conditions including rheumatoid and psoriatic arthritis, plaque psoriasis, Crohn’s disease and ulcerative colitis.

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biosimilars