Secukinumab administration by pre-filled syringe: efficacy, safety and usability results from a randomized controlled trial in psoriasis (FEATURE)

被引:318
作者
Blauvelt, A. [1 ]
Prinz, J. C. [2 ]
Gottlieb, A. B. [3 ]
Kingo, K. [4 ]
Sofen, H. [5 ]
Ruer-Mulard, M. [6 ]
Singh, V. [7 ]
Pathan, R. [7 ]
Papavassilis, C. [8 ]
Cooper, S. [9 ]
机构
[1] Oregon Med Res Ctr, Portland, OR 97223 USA
[2] Univ Munich, Dept Dermatol & Allergol, Munich, Germany
[3] Tufts Med Ctr, Boston, MA USA
[4] Univ Tartu, Dept Dermatol & Venereol, EE-50090 Tartu, Estonia
[5] Univ Calif Los Angeles, Sch Med, Dept Med Dermatol, Los Angeles, CA USA
[6] Le Bateau Blanc Imm A, Ctr Med, Martigues, Bouches Du Rhon, France
[7] Novartis Healthcare Private Ltd, Hyderabad, Andhra Pradesh, India
[8] Novartis Pharma AG, Basel, Switzerland
[9] Novartis Pharmaceut, E Hanover, NJ USA
关键词
SEVERE PLAQUE PSORIASIS; DOUBLE-BLIND; TH17; INDUCTION; ANTIBODY; THERAPY; IL-17; CELLS;
D O I
10.1111/bjd.13348
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Background Secukinumab, a fully human anti-interleukin-17A monoclonal antibody, demonstrated efficacy and safety in moderate-to-severe plaque psoriasis when administered via subcutaneous injection. Self-administration by pre-filled syringe (PFS) can offer patients clinical benefits of a drug, with increased convenience. Objectives To assess efficacy, safety and usability of secukinumab administration via PFS in subjects with moderate-to-severe plaque psoriasis. Materials and methods Subjects in this phase 3 trial were randomized 1 : 1 : 1 to secukinumab 300 or 150 mg or matching placebo. Results to week 12 are presented here. Each treatment was delivered using a PFS once weekly to week 4, and again at week 8. Co-primary endpoints were secukinumab superiority over placebo for week 12 PASI 75 (>= 75% reduction in Psoriasis Area and Severity Index) and IGA mod 2011 (2011 modified Investigator's Global Assessment) 0/1 response rates. Secondary endpoints included PFS usability, determined by observer rating of successful, hazard-free self-injection and subject rating of acceptability by the Self-Injection Assessment Questionnaire (SIAQ). Results Co-primary endpoints were met, with demonstration of superiority for each secukinumab dose vs. placebo at week 12 (PASI 75: 75.9%, 69.5% and 0% for secukinumab 300 mg, 150 mg and placebo; IGA mod 2011 0/1:69.0%, 52.5% and 0%, respectively; P < 0.0001 for all comparisons vs. placebo). PFS usability was high: 100% of subjects successfully self-administered treatment at week 1, and subjects reported high SIAQ-assessed acceptability of the PFS throughout the trial. No new/unexpected safety signals were observed. Conclusions Secukinumab administration by PFS was effective, with an acceptable safety profile and high usability. The PFS provides a reliable, convenient form of secukinumab administration in subjects with moderate-to-severe plaque psoriasis.
引用
收藏
页码:484 / 493
页数:10
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