For Healthcare Professionals

A Study of Baricitinib (LY3009104) in Participants From 1 Year to Less Than 18 Years Old With Systemic Juvenile Idiopathic Arthritis (sJIA)

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About the study

The reason for this study is to see if the study drug baricitinib is safe and effective in participants from 1 year to less than 18 years old with systemic juvenile idiopathic arthritis (sJIA). Participants are assigned to 1 of 2 cohorts. In cohort 1, participants will receive baricitinib or tocilizumab reference. In cohort 2, participants will receive baricitinib.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Participants must have a diagnosis of systemic Juvenile Idiopathic Arthritis (sJIA) as defined by International League of Associations for Rheumatology (ILAR) criteria with onset before the age of 16 years
  2. Participants must have at least 2 active joints at screening and baseline
  3. Cohort 1 (IL-6 inhibitor therapy naive): Participants who are at least 1 year and less than 18 years of age, except in countries that restrict use of tocilizumab in participants less than 2 years of age
  4. Cohort 2 (open-label baricitinib): Participants who are at least 1 year and less than 18 years of age

EXCLUSION CRITERIA

Exclusion Criteria:


  1. Participants must not have polyarticular JIA (positive or negative for rheumatoid factor), extended oligoarticular JIA, enthesitis-related JIA, or juvenile psoriatic arthritis
  2. Participants must not have persistent oligoarticular arthritis as defined by the ILAR criteria
  3. Participants must not have a history or presence of any autoimmune inflammatory condition other than JIA
  4. Participants must not have active anterior uveitis or are receiving concurrent treatment for anterior uveitis
  5. Participants must not have active fibromyalgia or other chronic pain conditions that, in the investigator's opinion, would make it difficult to appropriately assess disease activity for the purposes of this study
  6. Participants must not have biologic features of Macrophage Activation Syndrome (MAS) over the past 12 weeks
  7. Participants must not have a current or recent (<4 weeks prior to baseline) clinically serious infection
  8. Participants must not have a positive test for hepatitis B virus
  9. Participants must not have evidence of active tuberculosis (TB) or untreated latent TB

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 1-317-615-4559Email iconEmail Study Center

Study Details


Contition

Systemic Juvenile Idiopathic Arthritis

Age

1 - 17

Phase

PHASE3

Participants Needed

58

Est. Completion Date

May 31, 2026

Treatment Type

INTERVENTIONAL


Sponsor

Eli Lilly and Company

ClinicalTrials.gov NCT Identifier

NCT04088396

Study Number

I4V-MC-JAHU

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