EULAR 2019: Switching to our biosimilar not harmful to Humira patients, Sandoz shows

14 June 2019
sandoz_immunology_large

The Novartis (NOVN: VX) division Sandoz has added to the case for European prescribers to switch rheumatoid arthritis (RA) patients taking AbbVie's (NYSE: ABBV) Humira (adalimumab) to its biosimilar.

Data presented at EULAR from the Phase III ADMYRA trial shows that the efficacy and safety of Sandoz’s copy, branded Hyrimoz, matches that of the reference drug.

There were no clinically-meaningful differences between the two in patients with moderate-to-severe RA with inadequate response to disease modifying antirheumatic drugs, including methotrexate.

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

Today's issue

Company Spotlight





More Features in Biosimilars