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Nemoto, O.; Hirose, K.; Shibata, S.; Li, K.; Kubo, H.
British journal of dermatology (1951), March 2018, 2018-03-00, 20180301, Letnik: 178, Številka: 3Journal Article
Summary Background The interleukin (IL)‐23/IL‐17 pathway is central in the pathogenesis of psoriasis. The favourable efficacy and safety of guselkumab, an IL‐23‐specific monoclonal antibody, has been demonstrated in global phase III studies of plaque psoriasis. Objectives To evaluate the safety, efficacy and pharmacokinetics of single‐dose subcutaneous guselkumab in Japanese patients with moderate‐to‐severe plaque psoriasis. Methods Patients with ≥ 10% of total body surface area involvement and a Psoriasis Area and Severity Index (PASI) ≥ 12 were randomized (5 : 1) to receive guselkumab or placebo in four cohorts of this double‐blind, placebo‐controlled, single ascending‐dose, single‐centre study. Safety, pharmacokinetics and clinical response were monitored at baseline and specific time points over a 24‐week follow‐up period. Results To week 24, 55% (11/20) of patients in the guselkumab group and 50% (2/4) in the placebo group experienced ≥1 adverse event (AE). No deaths, serious AEs or AEs leading to treatment discontinuation were reported. Maximum clinical response was seen at week 16 with PASI 75 (≥ 75% improvement from baseline PASI) response in two of five (10 mg), four of five (30 mg and 300 mg) and three of five (100 mg) patients; and PASI 90 (≥ 90% improvement from baseline PASI) in zero of five (10 mg), three of five (30 mg), two of five (100 mg) and three of five (300 mg) patients. Mean maximum serum concentration (Cmax) and area under the curve from time zero to infinity values increased in a dose‐proportional manner with a mean terminal half‐life of 15·6–17·6 days and median time to reach Cmax of 4–6 days. Conclusions Guselkumab was generally well‐tolerated and exhibited sustained high levels of clinical response in Japanese patients with moderate‐to‐severe psoriasis. What's already known about this topic? Interleukin (IL)‐23/IL‐17 is a major pathway underlying the pathogenesis of psoriasis. The favourable efficacy and safety of guselkumab, an IL‐23‐specific monoclonal antibody, has been demonstrated in global phase III studies of plaque psoriasis. What does this study add? A single dose of guselkumab was generally well‐tolerated and efficacious in Japanese patients with moderate‐to‐severe plaque‐type psoriasis Results support further development of guselkumab in Japanese patients with moderate‐to‐severe psoriasis. Respond to this article
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Leto | Faktor vpliva | Izdaja | Kategorija | Razvrstitev | ||||
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
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Vir: Osebne bibliografije
in: SICRIS
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