Tremfya (guselkumab) achieves US approval for subcutaneous induction in adults with ulcerative colitis, now the first and only IL-23 inhibitor with a fully subcutaneous regimen

Johnson & Johnson

19 September 2025 - Johnson & Johnson is initiating a head to head study seeking to demonstrate the superiority of Tremfya versus Skyrizi (risankizumab) in Crohn's disease, based on the confidence in the clinical profile.

Johnson & Johnson today announced that the US FDA has approved a subcutaneous induction regimen of Tremfya (guselkumab) for the treatment of adults with moderately to severely active ulcerative colitis.

Read Johnson & Johnson press release  

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , Registration