Phase 2 Psoriatic Arthritis Trial, Recruiting NCT06865105 Sponsor: AbbVie Condition: Psoriatic Arthritis
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Phase 2 Psoriatic Arthritis Trial, Recruiting

NCT06865105
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are willing and able to follow all the procedures required by the study.
  • You have been formally diagnosed with Psoriatic Arthritis (PsA) for at least 6 months before the screening visit, and your diagnosis meets a specific set of classification standards checked at screening.
  • You have active disease, meaning you have at least 3 tender joints and at least 3 swollen joints, confirmed at both your screening visit and the start of the study.
  • You have active plaque psoriasis (a skin condition causing scaly patches) and/or a documented history of it.
  • You have already tried 1 to 2 approved targeted treatments (biological or targeted synthetic medications) for PsA, but either could not tolerate them or they did not work well enough for you.

Who may not be able to join:

  • You have had major surgery within the 12 weeks before joining the study, or you plan to have major surgery during the study.
  • You currently have HIV, active Hepatitis B, active Hepatitis C, or active tuberculosis (TB).
  • You have an active skin condition other than psoriasis that could make it difficult to properly assess your skin during the study.
  • You have a history of fibromyalgia, any form of arthritis that started before age 17, or any other inflammatory joint disease besides PsA — such as rheumatoid arthritis, gout, lupus, or related conditions.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: ABBVIE INC., AbbVie

Phone: 844-663-3742

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
11 April 2025
Est. completion
1 December 2027

Where this trial is recruiting

🇨🇦 Canada 🇨🇿 Czechia 🇫🇷 France 🇭🇺 Hungary 🇵🇱 Poland 🇺🇸 United States

Primary endpoints

Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response; Number of Participants With Adverse Events (AEs)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov