Phase 2 Psoriatic Arthritis Trial, Recruiting
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:
- People who are willing to take part voluntarily, have been fully informed about the study, and agree to follow the study procedures by signing a consent form
- People who are male or female, aged between 18 and 70 years old at the time of signing the consent form
- People who have had psoriatic arthritis (a condition causing joint inflammation linked to psoriasis) for at least 3 months before signing the consent form
- People who currently have active joint problems, including at least 3 joints that are tender when touched and at least 3 joints that are visibly swollen
Who may not be able to join:
- People with a history of certain infections, as defined by the trial's specific guidelines (confirm with trial site)
- People who have certain medical conditions or disorders listed in the trial's guidelines (confirm with trial site)
- People who have a serious, uncontrolled, or unstable health condition affecting any organ in the body
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.
Contact this trial
Principal Investigator: yi liu, phD, West China School of Medicine
Phone: 13401466347
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
Where this trial is recruiting
Primary endpoints
Proportion of subjects achieving ACR20 at Week 12 of treatment.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.