Phase 4 Psoriatic Arthritis Trial, Recruiting NCT06864026 Sponsor: Eli Lilly and Company Condition: Psoriatic Arthritis
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Phase 4 Psoriatic Arthritis Trial, Recruiting

NCT06864026
Recruiting Phase 4

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 have been diagnosed with active psoriatic arthritis by a rheumatologist or other healthcare professional experienced in treating this condition.
  • People with a Body Mass Index (BMI) of 30 or above (classified as obese), or a BMI between 27 and below 30 (classified as overweight) who also have at least one of the following health conditions: high blood pressure, high cholesterol or triglycerides, type 2 diabetes, obstructive sleep apnea, or cardiovascular disease.
  • People who have been taking the medication ixekizumab for approximately 3 months (between 2 and 4 months) before the decision is made to add the study drug.
  • People who are able to begin the study drug (tirzepatide) within 30 days of the treatment decision being made.

Who may not be able to join:

  • People who have been taking ixekizumab for more than 4 months or fewer than 2 months.
  • People who have previously taken tirzepatide or any GLP-1 receptor agonist medication, such as dulaglutide, liraglutide, or semaglutide (for example, medications like Ozempic or Victoza).
  • People who are currently enrolled in another clinical trial.
  • People who have a known allergy or sensitivity to any ingredient in tirzepatide.
  • People with a personal or family history of a specific type of thyroid cancer called medullary thyroid cancer.
  • People who have a condition called Multiple Endocrine Neoplasia type 2 (a rare hormonal disorder).
  • People who have type 1 diabetes.
  • People who have ever had inflammation of the pancreas (pancreatitis), whether short-term or long-term.
  • People who have certain serious eye complications related to diabetes, including proliferative diabetic retinopathy, diabetic maculopathy, or a form of retinopathy requiring urgent treatment.
  • People who have a history of a dangerous diabetic emergency involving very high blood sugar levels (ketoacidosis or hyperosmolar state/coma).
  • People who have experienced a severe episode of low blood sugar without warning signs within the 6 months before the screening visit.
  • People who have a history of serious digestive or stomach problems, including slow stomach emptying (gastroparesis), severe acid reflux, chronic indigestion, or ongoing nausea and vomiting.

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 28 July 2026
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Principal Investigator: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST), Eli Lilly and Company

Phone: 1-317-615-4559

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 4
Registry
ClinicalTrials.gov
Start date
6 March 2025
Est. completion
1 November 2027

Where this trial is recruiting

Puerto Rico 🇺🇸 United States

Primary endpoints

Percentage of Participants Achieving Normalized Functioning Health Assessment Questionnaire - Disability Index (HAQ-DI) ≤0.5 at 12 Months of Therapy; Percentage of Participants Achieving at Least a 10% Weight Loss at 12 Months of Therapy

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: 28 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