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临床试验/EUCTR2017-002464-40-GB
EUCTR2017-002464-40-GB进行中(未招募)1 期

A Phase 3, Randomized, Double-Blind Study Comparing Risankizumab to Placebo in Subjects with Active Psoriatic Arthritis Including Those Who Have a History of Inadequate Response or intolerance to Biologic Therapy(ies) (KEEPsAKE 2)

AbbVie Deutschland GmbH & Co. KG0 个研究点目标入组 420 人开始时间: 2018年11月27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
420

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

性别
All

入选标准

  • Clinical diagnosis of PsA with symptom onset at least 6 months prior to the Screening Visit and fulfillment of the Classification Criteria for PsA (CASPAR) at Screening Visit.
  • Subject has active disease at Baseline
  • Diagnosis of active plaque psoriasis with at least one psoriatic plaque of = 2 centimeter (cm) diameter or nail changes consistent with psoriasis at Screening Visit.
  • o Subject has demonstrated an inadequate response or intolerance to biologic therapy(ies) or csDMARD therapy(ies).
  • 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 340
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 80

排除标准

  • Subject is considered by investigator, for any reason, to be an unsuitable candidate for the study.
  • Subject has a known hypersensitivity to risankizumab.

研究者

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