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Study design. Study design for (a) UltIMMa‐1 and UltIMMa‐2 post hoc analysis, full study design included a placebo arm 19 and (b) LIMMitless; OLE, open‐label extension; RCT, randomised controlled trial; RZB, risankizumab; UST, ustekinumab. aPatients weighing ≤100 kg received 45 mg UST, while patients weighing >100 kg received 90 mg UST, per label instructions.
