Tremfya (guselkumab) approved by U.S. Food and Drug Administration as the first selective interleukin-23 inhibitor for active psoriatic arthritis

Janssen

14 July 2020 - In two Phase 3 clinical trials, Tremfya significantly improved signs and symptoms in joints, skin and soft tissue in adults with active psoriatic arthritis.

The Janssen Pharmaceutical Companies of Johnson & Johnson today announced that the U.S. FDA has approved Tremfya (guselkumab) for adult patients with active psoriatic arthritis (PsA), a chronic progressive disease characterised by painful joints and skin inflammation. 

Tremfya is the first treatment approved for active PsA that selectively inhibits interleukin (IL)-23, a naturally occurring cytokine that is involved in normal inflammatory and immune responses associated with the symptoms of PsA.

Read Janssen press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US