医学
头皮
安慰剂
银屑病
多中心研究
不利影响
皮肤病科
斑块性银屑病
内科学
双盲
随机对照试验
外科
病理
替代医学
作者
Kurt Gebauer,Lynda Spelman,Paul S. Yamauchi,Jerry Bagel,Tushar Nishandar,Michael Crane,Iris Kopeloff,Mudgal Kothekar,Siu‐Long Yao,Howard Sofen
标识
DOI:10.1016/j.jaad.2024.03.025
摘要
Background Scalp psoriasis is common and difficult to treat. Objective To evaluate efficacy and safety of tildrakizumab for the treatment of scalp psoriasis. Methods In this Phase 3b, randomized, double-blind, placebo-controlled study (NCT03897088), patients with moderate-to-severe plaque psoriasis affecting the scalp (Investigator Global Assessment modified [IGA mod] 2011 [scalp] ≥3, Psoriasis Scalp Severity Index [PSSI] ≥12, ≥30% scalp surface area affected) received tildrakizumab 100 mg or placebo at W0 and W4. The primary endpoint was IGA mod 2011 (scalp) score of "clear" or "almost clear" with ≥2-point reduction from baseline at W16 (IGA mod 2011 [scalp] response). Key secondary endpoints were PSSI 90 response at W12 and W16 and IGA mod 2011 (scalp) response at W12. Safety was assessed from adverse events. Results Of patients treated with tildrakizumab (n = 89) vs placebo (n = 82), 49.4% vs 7.3% achieved IGA mod 2011 (scalp) response at W16 (primary endpoint) and 46.1% vs 4.9% at W12; 60.7% vs 4.9% achieved PSSI 90 response at W16 and 48.3% vs 2.4% at W12 (all P <0.00001). No serious treatment-related adverse events occurred. Limitations Only short-term data are presented. Conclusion Tildrakizumab was efficacious for the treatment of scalp psoriasis with no new safety signals.
科研通智能强力驱动
Strongly Powered by AbleSci AI