Mallinckrodt (NYSE: MNK) reported that all primary and secondary outcome measures were met in its Phase IV study of Acthar Gel (repository corticotropin injection) in persistently active rheumatoid arthritis (RA) patients previously treated with disease-modifying anti-rheumatic drugs and corticosteroids.
The results, presented at the EULAR congress, showed that 63% of patients with persistently active RA achieved low disease activity at week 12, with Acthar offering significant improvements on placebo in multiple measures.
Acthar Gel is US Food and Drug Administration-approved as adjunctive therapy for short-term administration in RA, including for juvenile patients.
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