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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.
Bodemer, C; Kaszuba, A; Kingo, K; Tsianakas, A; Morita, A; Rivas, E; Papanastasiou, P; Keefe, D; Patekar, M; Charef, P; Zhang, L; Cafoncelli, S; Papavassilis, C.
Afiliação
  • Bodemer C; Department of Dermatology, Hôpital Necker-Enfants Malades, APHP, Paris, France.
  • Kaszuba A; DERMED Medical Services, Lodz, Poland.
  • Kingo K; Tartu University Hospital and University of Tartu, Tartu, Estonia.
  • Tsianakas A; Fachklinik Bad Bentheim, Bad Bentheim, Germany.
  • Morita A; Nagoya City University Hospital, Aichi, Japan.
  • Rivas E; Dermos, Guatemala City, Guatemala.
  • Papanastasiou P; Novartis Pharma AG, Basel, Switzerland.
  • Keefe D; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Patekar M; Novartis Pharma AG, Basel, Switzerland.
  • Charef P; Novartis Pharma AG, Basel, Switzerland.
  • Zhang L; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Cafoncelli S; Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
  • Papavassilis C; Novartis Pharma AG, Basel, Switzerland.
J Eur Acad Dermatol Venereol ; 35(4): 938-947, 2021 Apr.
Article em En | MEDLINE | ID: mdl-33068444
ABSTRACT

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase / Anticorpos Monoclonais Tipo de estudo: Clinical_trials Limite: Adult / Child / Humans Idioma: En Revista: J Eur Acad Dermatol Venereol Assunto da revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase / Anticorpos Monoclonais Tipo de estudo: Clinical_trials Limite: Adult / Child / Humans Idioma: En Revista: J Eur Acad Dermatol Venereol Assunto da revista: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França