Sandoz, the generic medicines unit of Swiss drug major Novartis (NOV: N), has released new data bolstering its case for regulatory approval for its biosimilar adalimumab.
The one-year study comparing the biosimilar with its reference biologic Humira (adalimumab), from AbbVie (NYSE: ABBV), showed that efficacy and safety profiles in moderate-to-severe chronic plaque psoriasis were comparable.
Results were presented at the 26th Congress of the European Academy of Dermatology and Venereology in Geneva, Switzerland.
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