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临床试验/EUCTR2013-001417-32-HU
EUCTR2013-001417-32-HU进行中(未招募)1 期

A Multicenter, Randomized, Double-blind, Parallel Group Study of CNTO 136 (sirukumab) Administered Subcutaneously as Monotherapy Compared With Adalimumab Monotherapy, in Subjects with Active Rheumatoid Arthritis - SIRROUND-H

Janssen-Cilag International N.V.0 个研究点目标入组 510 人开始时间: 2014年3月17日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
510

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

  • 1. Have a diagnosis of rheumatoid arthritis (RA) for at least 6 months before screening
  • 2. Have moderately to severely active RA with at least 8 of 68 tender joints and 6 of 66 swollen joints, at screening and at baseline
  • 4. Have previous or current treatment with methotrexate (MTX) and are considered intolerant to MTX (including MTX-naive subjects for whom it is inappropriate to administer MTX), and/or are considered inappropriate for treatment with MTX, and/or an inadequate responder to methotrexate
  • 5. Must not have received MTX or any other non-biologic DMARD including but not limited to sulfasalazine, hydroxychloroquine, chloroquine, and bucillamine for at least 2 weeks prior to the first administration of the study agent
  • 6. C-reactive protein >= 10.00 mg/L or erythrocyte sedimentation rate >=28 mm/hr at screening
  • 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 423
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 87

排除标准

  • 1. Has Functional Class IV as defined by the ACR Classification of Functional Status in Rheumatoid Arthritis
  • 2. Has ever received biologic therapy for RA, including but not limited to the following: TNF-alpha inhibitors, tocilizumab, rituximab, anakinra, abatacept
  • 3. Has ever used tofacitinib therapy or any other JAK inhibitor
  • 4. Has received intra-articular, intramuscular, or IV corticosteroids for RA, including adrenocorticotrophic hormone during the 4 weeks prior to first study agent administration
  • 5. Has received leflunomide within 24 months before the first study agent administration and has not undergone a drug elimination procedure, unless the M1 metabolite is measured and is undetectable

研究者

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