Novartis’ Sandoz scores EU approval for Remicade biosimilar

The European Commission has given its approval to Sandoz, Novartis’ generics and biosimilars unit, for its biosimilar version of Janssen’s Remicade (infliximab) and other products, known as Zessly.
The therapy has been authorised in all the indications of its reference product, which includes the treatment of rheumatoid arthritis, adult Crohn’s disease, paediatric Crohn’s disease, adult ulcerative colitis, paediatric ulcerative colitis, ankylosing spondylitis, psoriatic arthritis and plaque psoriasis.
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