Secukinumab demonstrates high efficacy and a favourable safety profile in paediatric patients with severe chronic plaque psoriasis: 52-week results from a Phase 3 double-blind randomized, controlled trial

被引:70
作者
Bodemer, C. [1 ]
Kaszuba, A. [2 ]
Kingo, K. [3 ,4 ]
Tsianakas, A. [5 ]
Morita, A. [6 ]
Rivas, E. [7 ]
Papanastasiou, P. [8 ]
Keefe, D. [9 ]
Patekar, M. [8 ]
Charef, P. [8 ]
Zhang, L. [9 ]
Cafoncelli, S. [9 ]
Papavassilis, C. [8 ]
机构
[1] Hop Necker Enfants Malad, AP HP, Dept Dermatol, Paris, France
[2] DERMED Med Serv, Lodz, Poland
[3] Tartu Univ Hosp, Tartu, Estonia
[4] Univ Tartu, Tartu, Estonia
[5] Fachklin Bad Bentheim, Bad Bentheim, Germany
[6] Nagoya City Univ Hosp, Nagoya, Aichi, Japan
[7] Dermos, Guatemala City, Guatemala
[8] Novartis Pharma AG, Basel, Switzerland
[9] Novartis Pharmaceut, E Hanover, NJ USA
关键词
D O I
10.1111/jdv.17002
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Secukinumab has demonstrated sustained long-term efficacy with a favourable safety profile in various psoriatic disease manifestations in adults. Objectives Here, the efficacy and safety of two secukinumab dosing regimens [low dose (LD) and high dose (HD)] in paediatric patients with severe chronic plaque psoriasis over one year are reported. Methods In this multicentre, double-blind study (NCT02471144), patients aged 6 to <18 years with severe chronic plaque psoriasis were stratified and randomized by weight (<25 kg, 25 to <50 kg, >= 50 kg) and age (6 to <12 years, 12 to <18 years) to receive low-dose (LD: 75/75/150 mg) or high-dose (HD: 75/150/300 mg) subcutaneous secukinumab or placebo or etanercept 0.8 mg/kg (up to a max of 50 mg). Results Overall, 162 patients were randomized to receive secukinumab LD (n = 40) or HD (n = 40), etanercept (n = 41) or placebo (n = 41). The co-primary objectives of the study were met with both secukinumab doses (LD and HD) showing superior efficacy compared to placebo (P < 0.0001) with respect to PASI 75 response (80.0%, 77.5% vs. 14.6%) and IGA mod 2011, 0 or 1 response (70%, 60% vs. 4.9%) at Week 12. Both secukinumab doses were superior to placebo (P < 0.0001) with respect to PASI 90 response at Week 12 (72.5%, 67.5% vs. 2.4%). The efficacy of both doses was sustained to Week 52 with secukinumab achieving higher responses vs. etanercept (PASI 75/90/100: LD, 87.5%/75.0%/40.0% and HD, 87.5%/80.0%/47.5.% vs. etanercept, 68.3%/51.2%/22.0% and IGA 0 or 1: LD, 72.5% and HD, 75.0% vs. etanercept, 56.1%). The safety profile of secukinumab was consistent with the adult Phase 3 studies, with no new safety signals identified. Conclusions Both doses of secukinumab demonstrated high and sustained efficacy up to Week 52 with a favourable safety profile in paediatric patients with severe chronic plaque psoriasis.
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页码:938 / 947
页数:10
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