Phase 4 Psoriasis Trial, Recruiting NCT06857942 Sponsor: Eli Lilly and Company Condition: Psoriasis
Back to Psoriasis

Phase 4 Psoriasis Trial, Recruiting

NCT06857942
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 moderate-to-severe plaque psoriasis by a dermatologist or other qualified clinician experienced in treating psoriasis
  • People with a body mass index (BMI) of 30 or above (classified as obese), or a BMI between 27 and under 30 (classified as overweight) alongside at least one weight-related health condition such as high blood pressure, abnormal cholesterol levels, type 2 diabetes, obstructive sleep apnea, or heart/cardiovascular disease
  • People who started treatment with ixekizumab approximately 3 months before the decision to add the second study medication (within a window of 2 to 4 months)
  • People who are able to begin the second study medication within 30 days of the initial screening visit

Who may not be able to join:

  • People who have been receiving ixekizumab for more than 4 months or less than 2 months at the time of the decision to add the second medication
  • People who have previously used tirzepatide or similar medications known as GLP-1 receptor agonists, such as dulaglutide, liraglutide, or semaglutide
  • People who are currently participating in another clinical trial
  • People with a known allergy or sensitivity to tirzepatide or any of its ingredients
  • People with a personal or family history of a specific type of thyroid cancer called medullary thyroid cancer
  • People with a condition called multiple endocrine neoplasia type 2 (a rare hormonal disorder)
  • People with type 1 diabetes
  • People who have had inflammation of the pancreas (pancreatitis), either in the past or currently
  • People with certain serious eye complications related to diabetes, including proliferative diabetic retinopathy, diabetic maculopathy, or a form of nonproliferative diabetic retinopathy that requires immediate treatment
  • People with a history of a dangerous condition called diabetic ketoacidosis or a hyperosmolar state/coma (serious diabetes-related emergencies)
  • People who have experienced severe low blood sugar episodes or who are unaware when their blood sugar drops dangerously low, within the 6 months before screening
  • People with a history of serious stomach or digestive problems, including delayed stomach emptying (gastroparesis), severe acid reflux, persistent indigestion, or chronic nausea, constipation, or 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 22 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
19 March 2025
Est. completion
1 May 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Percentage of Participants Achieving Dermatology Life Quality Index (DLQI) (0,1); Percentage of Participants Achieving at least 10% Weight Reduction

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: 22 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