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Patients with plaque psoriasis need more effective, safer, and more convenient biological treatments to improve their quality of life
.
Risankizumab and Suckinumab inhibit interleukin (IL)-23 and IL-17A, respectively, and are effective for adult patients with moderate to severe plaque psoriasis, but the dosage regimen is different
The study aims to directly compare the efficacy and safety of risankizumab and seckinumab within 52 weeks
.
Adult patients with chronic, moderate, and severe plaque psoriasis were randomly divided into Risankizumab 150 mg or Suckinumab 300 mg treatment groups at a ratio of 1:1, 30 cases in each group, and randomly divided into two groups, 30 cases in each group, respectively.
The main observation index is the proportion of patients whose psoriasis area severity index (≥90) was improved by 90% at the 16th week (non-inferiority comparison, 12% difference) and 52 weeks (advantage comparison)
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Results 327 patients from 9 countries received risankizumab (n=164) or seckinumab (n=163) treatment
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The proportion of patients with risankizumab reaching PASI90 at week 16 [73.
Conclusion: At 52 weeks of treatment, risankizumab showed superior efficacy and similar safety to seckinumab, but the frequency of medication was lower than that of seckinumab
.
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Literature source: Warren RB, Blauvelt A, Poulin Y, Efficacy and safety of risankizumab vs.
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