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临床试验/EUCTR2016-004573-40-ES
EUCTR2016-004573-40-ES进行中(未招募)1 期

Multi-center, double-blind, randomised, placebo-controlled, phase IIa study to investigate efficacy, safety, tolerability, pharmacokinetics and pharmacogenomics of multiple intravenous doses of BI 655130 in patients with Palmoplantar Pustulosis (PPP)

Boehringer Ingelheim España, S.A.0 个研究点目标入组 79 人开始时间: 2017年3月2日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
79

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

入选标准

  • - Male or female patients, 18 to 65 years of age at screening.
  • - Palmoplantar Pustulosis
  • - Further criteria apply
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 55
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 5

排除标准

  • - Patients with associated plaque psoriasis = 10% of the body surface area.
  • - Presence or known history of anti-TNF-induced PPP-like disease.
  • - Active or latent tuberculosis
  • - Further criteria apply

研究者

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