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临床试验/CTIS2023-505477-33-00
CTIS2023-505477-33-00招募中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) - M15-998

AbbVie Deutschland GmbH & Co. KG0 个研究点目标入组 333 人开始时间: 2024年1月19日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
333

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
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., Subject has demonstrated an inadequate response or intolerance to biologic therapy(ies) or csDMARD therapy(ies).

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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