CClinicalTrials.gg
CompletedNCT03769558Updated Mar 20, 2020

A Study of Juvenile Idiopathic Arthritis Patients Given Abatacept and the Number of Infections or Malignancies That Occur

An observational study in Juvenile Idiopathic Arthritis, sponsored by Bristol-Myers Squibb. Completed at 1 site in United States. Open to participants aged 12 Months and older. Per ClinicalTrials.gov, last updated 2020-03-20.

Sponsored by Bristol-Myers Squibb · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
264
Ages
12 Months and older
Sex
All
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Study summary

This study will determine the incidences of infections and malignancies among JIA patients treated with abatacept

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Conditions studied

  • Juvenile Idiopathic Arthritis
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In context

Arthritis

3,554 studies on the registry are indexed under Arthritis; 317 are open to participants now.

This study's enrollment of 264 is above the median of 155 across 1,057 observational studies indexed under Arthritis.

Browse Arthritis studies →

Lead sponsor

Bristol-Myers Squibb is the lead sponsor of 1,538 studies on the registry; 116 are open to participants now.

Of its 429 completed or terminated interventional studies of FDA-regulated products, 223 (52%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
12 Months and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The study population will include all patients with JIA who are treated with abatacept

Inclusion criteria

  • Two diagnoses of JIA (ICD-9 code 714.3x) within 90 days
  • Age less than 18 years at the time of second of the two diagnoses
  • Index date is the date of initiating treatment with abatacept

Exclusion criteria

Exclusion Criteria:

  • Greater than or equal to 18 years of age
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
264 participants (actual)
Patient registry
No

Groups and cohorts

  • JIA patients prescribed abatacept

    Other: Non-Interventional

Interventions

  • OtherNon-Interventional

    Non-Interventional

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What researchers measure

Primary outcomes

  1. Incidence of infections

    Time frame: 110 months

Secondary outcomes

  1. Incidence of malignancies

    Time frame: 110 months

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Study locations

1 site
  • Local Institution
    Princeton, New Jersey 08540, United States
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 20, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03769558
Lead sponsor
Bristol-Myers Squibb
Responsible party
Sponsor
First posted
Dec 7, 2018
Start date
Jul 12, 2016
Primary completion
Sep 30, 2016
Completion
Sep 30, 2016
Last update
Mar 20, 2020

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2020. You cannot join it, but the record below documents what was studied.

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