Ultomiris recommended for EU approval for gMG
25 July 07:05 BST Ultomiris recommended for approval in the EU by CHMP for the treatment of adults with generalised myasthenia gravis First and only long-acting C5 complement inhibitor showed early effect and demonstrated clinical improvement in activities of daily living Ultomiris (ravulizumab) has been recommended for marketing authorisation in the European Union (EU) as an add-on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gMG) who are anti-acetylcholine receptor (AChR) antibody-positive. If authorised, Ultomiris would be the first