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临床试验/EUCTR2018-003351-37-HU
EUCTR2018-003351-37-HU进行中(未招募)1 期

A Randomized, Active Controlled, Parallel Group, Phase 3b/4 Study of Baricitinib in Patients with Rheumatoid Arthritis. - RA-BRIDGE

Eli Lilly and Company0 个研究点目标入组 2,600 人开始时间: 2019年7月24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
2,600

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

  • Participants must have an inadequate response or intolerance to at least 1 disease-modifying antirheumatic drugs (DMARD) (synthetic or biologic).
  • Participants must have at least one of the following characteristics:
  • Documented evidence of a VTE prior to this study
  • At least 60 years of age or older
  • A body mass index (BMI) greater than or equal to 30 kilograms per meter squared (kg/m2), or
  • Age 50 to less than 60 years AND BMI 25 to less than 30 kg/m2.
  • 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 2080
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 520

排除标准

  • Participants must not have any problems taking a tumor necrosis factor (TNF) inhibitor.
  • Participants must not be pregnant or breastfeeding.
  • Participants must not have had more than one VTE.
  • Participants must not have cancer.
  • Participants must not have active herpes zoster, serious infection, active tuberculosis, or any other serious illness.
  • Participants must not have had a live vaccine within four weeks of study start.
  • Participants must not have participated in any other clinical trial within four weeks of study randomisation
  • Participants must not have a history of IV drug use, other illicit drug abuse, or chronic alcohol abuse in the past year.

研究者

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