Autoimmune diseases specialist argenx (Nasdaq: ARGX) has previously referred to Vyvgart (efgartigimod alfa-fcab), an antibody fragment that binds to the neonatal Fc receptor (FcRn), as a ‘pipeline in a product’.
The Belgo-Dutch company had a further chance to demonstrate this with a presentation in the plenary session at the American Society of Hematology (ASH) Annual Meeting and Exposition in New Orleans over the weekend.
This presentation was on data from argenx’ Phase III ADVANCE study, the first of two registrational trials evaluating the efficacy, safety and tolerability of Vyvgart for the treatment of adults with primary ITP, this time the intravenous formulation.
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