A Phase 3, Randomized, Double-Blind Study comparing ABT-494 to Placebo in Subjects with Moderately to Severely Active Rheumatoid Arthritis Who are on a Stable Dose of Conventional Synthetic Disease-Modifying Anti-Rheumatic Drugs (csDMARDs) and Have an Inadequate Response to csDMARDs

  • STATUS
    Recruiting
  • sponsor
    Abbvie
Updated on 23 November 2020

Summary

A Phase 3, Randomized, Double-Blind Study comparing ABT-494 to Placebo in Subjects with Moderately to Severely Active Rheumatoid Arthritis Who are on a Stable Dose of Conventional Synthetic Disease-Modifying Anti-Rheumatic Drugs (csDMARDs) and Have an Inadequate Response to csDMARDs

Description

Participation in this research study would last approximately 24 weeks and would include at least 11 visits to our office. Compensation up to $75 per visit may be provided for time and travel.

For more info please contact our office

Details
Clinical Study IdentifierTX144796
SponsorAbbvie
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Are at least 18 years of age
Have been diagnosed with rheumatoid arthritis ≥ 3 months

Exclusion Criteria

Have never received a JAK inhibitor (ex. Xeljanz, barcitinib, or filgotinib)
No history of drug or alcohol abuse within the last 6 months
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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