A phase III open-label, randomized multicenter study to evaluate efficacy and safety of secukinumab in pediatric patients with moderate to severe plaque psoriasis: 24-week results
Journal of the American Academy of Dermatology Sep 23, 2021
Magnolo N, Kingo K, Laquer V, et al. - In pediatric patients with moderate-to-severe plaque psoriasis, secukinumab dosing regimens were both effective and well-tolerated.
It was a Phase-III, open-label, randomized, multicenter-study.
At Week-12, both secukinumab doses (low dose: 75/75/150 mg and high dose: 75/150/300 mg) outperformed the historical placebo in terms of PASI 75/90 and IGA0/1 responses.
The estimated probability of a positive treatment effect (ie, log-Odd Ratio [OR] > 0) for secukinumab low or high dose vs historical placebo is 1 (ie, 100%).
At Week-12, the IGA0/1 response rates were 78.6% and 83.3%, respectively, and the PASI90 response rates were 69% and 76.2%, respectively; the PASI75 response rate was 92.9% for both dosages.
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