Last updated on July 2018

A Phase 3, Randomized, Double-Blind Study Comparing ABT-494 to Placebo on Stable Conventional Synthetic Disease-Modifying Anti-Rheumatic Drugs (csDMARDs) in Subjects with Moderately to Severely Active Rheumatoid Arthritis with Inadequate Response or Intolerance to Biologic DMARDs (bDMARDs)


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Rheumatoid Arthritis
  • Age: 18 Years
  • Gender: Male or Female

Inclusion Criteria:

  • Diagnosis of RA for ≥ 3 months who also fulfill either the 1987-revised ACR classification criteria
  • or the 2010 ACR/EULAR classification criteria for RA.
  • Subjects have been treated for ≥ 3 months with ≥ 1 bDMARD therapy, but continue to exhibit active RA or had to discontinue due to intolerability or toxicity.
  • Subjects have been receiving csDMARD therapy ≥ 3 months and on a stable dose for ≥ 4 weeks prior to the first dose of study drug.

Exclusion Criteria:

  • Prior exposure to any Janus kinase (JAK) inhibitor.
  • History of inflammatory joint disease other than RA

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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