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Avtozma was FDA-approved in January 2025 to treat the same conditions as the reference product Actemra (tocilizumab).
October 2, 2025
By: Rachel Klemovitch
Assistant Editor
Celltrion, Inc. announced that Avtozma (tocilizumab-anoh) intravenous (IV) formulation is now available to patients in the United States. Avtozma IV is approved for all same indications as the reference product Actemra (tocilizumab), including rheumatoid arthritis (RA), giant cell arteritis (GCA), polyarticular juvenile idiopathic arthritis (PJIA), systemic juvenile idiopathic arthritis (SJIA), coronavirus disease (COVID-19), and cytokine release syndrome (CRS). Avtozma IV will be availab...
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