FDA expands use of Genentech's Actemra to include polyarticular JIA

Genentech received approval from the FDA to market Actemra, or tocilizumab, for children 2 and older with active polyarticular juvenile idiopathic arthritis. The drug, a humanized interleukin-6 receptor antagonist, can be given alone or with methotrexate. The approval was based on data from a late-stage trial showing that the drug improved symptoms in children with the condition.

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