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临床试验/EUCTR2015-002433-22-EE
EUCTR2015-002433-22-EE进行中(未招募)1 期

A Phase 3, Multicenter Study with a 36-Week Open-Label Period Followed by a Randomized Double-Blind Withdrawal Period from Week 36 to Week 104 to Evaluate the Long Term Efficacy and Safety of Ixekizumab (LY2439821) 80 mg Every 2 Weeks in Biologic Disease-Modifying Antirheumatic Drug–Naive Patients with Active Psoriatic Arthritis

Eli Lilly and Company0 个研究点目标入组 400 人开始时间: 2015年9月14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
400

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

  • Patients are eligible to be included in the study only if they meet all of the following criteria:
  • [1] are male or female patients 18 years or older who agree to use reliable method of birth control or remain abstinent during the study
  • [2] have had diagnosis of active PsA for at least 6 months and meet Classification for Psoriatic Arthritis (CASPAR) criteria
  • [3] active PsA defined as the presence of at least 3 tender and at least 3 swollen joints
  • [4] have been treated with 1 or more conventional disease-modifying antirheumatic drugs (DMARDs)
  • [5] have active psoriatic skin lesions (plaque) or a documented history of plaque psoriasis
  • 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 380
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • Patients will be excluded from study enrollment if they meet any of the following criteria:
  • [7] have received any previous treatment or are currently receiving treatment with any biologic or small-molecule therapy for PsA or psoriasis
  • [10] have had, in the opinion of the investigator, inadequate response to treatment with =4 cDMARDs or immune modifiers
  • [12] are receiving treatment with more than 1 cDMARD
  • [20] have a known allergy or hypersensitivity to any biologic therapy that would pose an unacceptable risk to the patient if participating in this study
  • [24] have a diagnosis of other inflammatory arthritic syndromes such as RA, ankylosing spondylitis, reactive arthritis, or enteropathic arthritis
  • [33] have serious disorder other than psoriatic arthritis
  • [36] had a serious infection within 12 weeks
  • [43] are positive for human immunodeficiency virus serology
  • [44] have evidence of or test positive for hepatitis B or hepatitis C virus
  • [50] are women who are lactating or breastfeeding

研究者

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