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临床试验/NCT03773965
NCT03773965招募中3 期

A Phase 3 Multicenter Study to Evaluate the Long-Term Safety and Efficacy of Baricitinib in Patients From 1 Year to <18 Years of Age With Juvenile Idiopathic Arthritis (JIA)

Eli Lilly and Company93 个研究点 分布在 18 个国家目标入组 190 人开始时间: 2019年4月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
入组人数
190
试验地点
93
主要终点
Number of Participants with One or More Serious Adverse Event(s) (SAEs)

研究概览

简要总结

The reason for this study is to see if the study drug baricitinib is safe and effective in the treatment of JIA in participants ages 1 to 17. This study is for participants that have been enrolled in studies I4V-MC-JAHV (NCT03773978) or I4V-MC-JAHU.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Year 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Participants must have completed a previous study of baricitinib for the treatment of JIA.

排除标准

  • Participants must not have had a permanent discontinuation of baricitinib in the prior study.
  • Participants must have not developed an allergy to baricitinib.

研究组 & 干预措施

Baricitinib

Experimental

Baricitinib given orally.

干预措施: Baricitinib (Drug)

结局指标

主要结局

Number of Participants with One or More Serious Adverse Event(s) (SAEs)

时间窗: Baseline through Week 264

Number of participants with one or more SAEs

Number of Participants with Permanent Investigational Product Discontinuations

时间窗: Baseline through Week 264

Number of participants with permanent investigational product discontinuations

次要结局

  • Change from Baseline in Spondyloarthritis Research Consortium of Canada (SPARCC) Enthesitis Index(Baseline, Week 264)
  • Change from Baseline in Juvenile Spondyloarthritis Disease Activity Index (JSpADA)(Baseline, Week 264)
  • Change from Baseline in Immunoglobulin Levels(Baseline, Week 264)
  • Change from Baseline in Immunophenotyping (T Cells)(Baseline, Week 264)
  • Change of Immunoglobulin G (IgG) Titers(Pre-Vaccination to 12 Weeks Post-Vaccination)
  • Proportion of Participants with Inactive Disease(Week 264)
  • Proportion of Participants with Minimal Disease Activity(Week 264)
  • Proportion of Participants in Remission(Week 264)
  • Change from Baseline in Juvenile Arthritis Disease Activity Score-27 (JADAS27)(Baseline, Week 264)
  • Change from Baseline in Arthritis-Related Pain Severity as Measured by the Childhood Health Assessment Questionnaire (CHAQ) Pain Visual Analog Scale (VAS) Item(Baseline, Week 264)
  • Change from Baseline in Psoriasis Area and Severity Index (PASI)(Baseline, Week 264)
  • Proportion of Participants Achieving Pediatric American College of Rheumatology 30 Responder Index (PedACR30)(Week 264)
  • Proportion of Participants who have Disease Flare(Baseline through Week 264)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (93)

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