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A Study of Baricitinib in Participants With Rheumatoid Arthritis

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NCT04086745 · results posted

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →. With Incyte Corporation.

Phase
Phase 4
Status
Completed
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
1,050actual
Sites
119
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2020-02-14actualWhen the study began enrolling
Primary completion2025-05-19actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-05-19actualThe whole study's end, after follow-up
First posted2019-09-12actualWhen this record first appeared on the registry
Results posted2026-07-10actualWhen the sponsor posted results to the registry
Record updated2026-07-10actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Rheumatoid Arthritis

Interventions

  • Drug: Baricitinib — also filed as LY3009104
  • Drug: TNF Inhibitor — also filed as Etanercept, Adalimumab

Primary outcome

what the primary-completion date above is the date OF
Pooled JAJA and JAJD: Time From First Dose of Study Treatment to First Event of Venous Thromboembolism (VTE) [Combined Baricitinib Dose Versus TNF Inhibitor]
measured From the first dose of study treatment up to 30 days after the last dose or the last study visit, whichever occurs first (approximately up to 6.1 years for JAJA and 5.3 years for JAJD participants)

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2024-03-22 · 1.5 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-07-21 · 1.3 MB · SAP_001.pdf

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