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A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study Evaluating the Efficacy and Safety of Baricitinib (LY3009104) in Patients With Moderately to Severely Active Rheumatoid Arthritis Who Have Had an Inadequate Response to Tumor Necrosis Factor Inhibitors

Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study Evaluating the Efficacy and Safety of Baricitinib (LY3009104) in Patients With Moderately to Severely Active Rheumatoid Arthritis Who Have Had an Inadequate Response to Tumor Necrosis Factor Inhibitors

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 09 Nov 2020

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At a glance

  • Drugs Baricitinib (Primary)
  • Indications Rheumatoid arthritis
  • Focus Registrational; Therapeutic Use
  • Acronyms RA-BEACON
  • Sponsors Eli Lilly and Company; Lilly Korea
  • Most Recent Events

    • 06 Jun 2020 Results of an analysis assessing number needed to treat (NNT) to report improvements minimum clinically important differences in multiple patient-reported outcomes at week 12 after treatment with Baricitinib 4mg in RA-BEAM and BARI 2 mg or BARI 4 mg in RA-BEACON studies presented at the 21st Annual Congress of the European League Against Rheumatism
    • 15 Jun 2019 Results of pooled analysis from nine studies of Baricitinib treated rheumatoid arthritis patients presented at the 20th Annual Congress of the European League Against Rheumatism
    • 06 Jun 2019 According to an Eli Lilly media release, data from this trial will be presented at the upcoming Annual European Congress of Rheumatology (EULAR 2019) in Madrid from June 12-15, 2019.
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