EMA/CHMP recommends approval for six biosimilars

14 December 2024

The European Medicines Agency’s (EMA) human medicines committee (CHMP) adopted positive opinions for six biosimilar medicines at its December meeting.

First, was for South Korea’s Celltrion’ (KRX: 068270) Avtozma (tocilizumab), for the treatment of rheumatoid arthritis, systemic juvenile idiopathic arthritis, polyarticular juvenile idiopathic arthritis, giant cell arteritis, CAR-T cell-induced severe or life-threatening cytokine release syndrome and COVID-19.

Other Celltrion biosimilars recommended were

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