Celltrion has received a formal approval from the European Commission extending the marketing authorization for its Remsima SC (infliximab) subcutaneous biosimilar to cover an additional five indications on top of the rheumatoid arthritis indication for which it was initially approved.
The extension – covering the unique subcutaneous version of infliximab for the treatment of adult patients with ankylosing spondylitis, Crohn’s...






