Enrolling now · NCT06857942

A study testing whether a new weekly shot from Lilly, tirzepatide, can calm psoriasis.

What this means for you

Who can join
Adults 18+, have psoriasis, BMI 27+.
What you take
tirzepatide, given as part of the study at no cost to you. Some participants may receive a placebo (an inactive version) instead, decided at random.
How long it lasts
The full study runs about 3.2 years; your own time in it is usually shorter.
What you get
The study medication and study-related care at no cost. Compensation varies by study site; many cover travel and provide the study medication at no cost. The trial coordinator will explain what that site offers before you join.
Phase Phase 4Sponsor Eli Lilly and CompanyDrug tirzepatideClass GLP-1/GIPSites 40 USEnrollment target 200

What this study is for

Primary condition: Psoriasis. Also studied in: Overweight or Obesity.

Full scientific study title: A Study to Investigate the Effectiveness of Tirzepatide (LY3298176) Following Initiation of Ixekizumab (LY2439821) in Participants With Mode.

Who can join

Age18 and upSexAnyBMI27 or higher

Adults 18+, have psoriasis, BMI 27+. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.

Full medical eligibility (for you and your doctor)verbatim from the registry

This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.

Key inclusion criteria

  • Have a diagnosis of moderate-to-severe plaque PsO, as defined by a dermatologist or other experienced clinician treated PsO (for example, allergologist, nurse practitioner or physician assistant)
  • Have body mass index (BMI) of 30 kilograms per meter squared (kg/m²) or greater (obesity) or 27 kg/m² to <30 kg/m² (overweight) in the presence of at least 1 weight-related comorbid condition (hypertension, dyslipidemia, type 2 diabetes mellitus, obstructive sleep apnea, or cardiovascular diseases).
  • Must have initiated treatment with ixekizumab for approximately 3 months (± 1 month) prior to decision to add tirzepatide.
  • Must be able to initiate tirzepatide (Day 0) within 30 days of treatment decision (baseline/screening).

Key exclusion criteria

  • Have currently received ixekizumab for more than 4 months or less than 2 months.
  • Have had any exposure to tirzepatide or other glucagon-like peptide-1 receptor agonist (GLP-1 RAs), for example, dulaglutide, liraglutide, or semaglutide.
  • Are currently enrolled in any other clinical study.
  • Have a known hypersensitivity to tirzepatide or to any of its component.
  • Have a personal or family history of medullary thyroid cancer.

Where this study is enrolling

This trial has 40 sites across 22 states. Contact a site coordinator directly to start screening.

Arizona1 site
  • Medical Dermatology Specialists
    Phoenix, Arizona
    602-354-5770
California4 sites
  • First OC Dermatology Research Inc
    Fountain Valley, California
    714-531-2966
  • Center For Dermatology Clinical Research, Inc.
    Fremont, California
    510-797-0140
  • Metropolis Dermatology
    Los Angeles, California
    424-393-0005
  • Northridge Clinical Trials
    Northridge, California
    818-350-7482
Florida5 sites
  • NeoClinical Research
    Hialeah, Florida
    305-456-9062
  • Skin Care Research
    Hollywood, Florida
    954-674-3535
  • Encore Medical Research
    Hollywood, Florida
    954-400-1725
  • MOORE Clinical Research, Inc. d/b/a TrueBlue Clinical Research
    Tampa, Florida
    813-948-7550
  • TruDerm & TruSpa
    Wellington, Florida
Georgia1 site
  • Southeast Research Specialists
    Douglasville, Georgia
    678-702-3376
Indiana2 sites
  • Dawes Fretzin Clinical Research Group, LLC
    Indianapolis, Indiana
    317-516-5030
  • The Indiana Clinical Trials Center, PC
    Plainfield, Indiana
    317-837-6082
Kentucky1 site
  • Equity Medical - Bowling Green
    Bowling Green, Kentucky
    270-213-7777
Maryland1 site
  • Dermatology and Skin Cancer Specialists, LLC
    Rockville, Maryland
Massachusetts1 site
  • Metro Boston Clinical Partners
    Brighton, Massachusetts
Michigan3 sites
  • David Fivenson, MD, PLC
    Ann Arbor, Michigan
    734-222-9630
  • Great Lakes Research Group, Inc.
    Bay City, Michigan
    989-895-9100
  • The Derm Institute of West Michigan
    Caledonia, Michigan
    616-326-0114
Nevada1 site
  • Skin Cancer and Dermatology Institute - Reno
    Reno, Nevada
    775-336-3658
New Hampshire1 site
  • Stracskin
    Portsmouth, New Hampshire
    617-833-9995
New Jersey2 sites
  • Psoriasis Treatment Center of Central New Jersey
    East Windsor, New Jersey
  • Care Access - Hoboken
    Hoboken, New Jersey
    551-278-8680
New York1 site
  • Equity Medical
    New York, New York
    212-466-6550
North Carolina2 sites
  • Revival Research Institute, LLC
    Cary, North Carolina
  • Onsite Clinical Solutions - Huntersville
    Huntersville, North Carolina
    800-785-3150
Ohio1 site
  • Optima Research - Boardman
    Boardman, Ohio
    330-422-3234
Oregon1 site
  • Oregon Dermatology and Research Center
    Portland, Oregon
    503-226-3376
Pennsylvania1 site
  • Dermatology Associates of Plymouth Meeting
    Plymouth Meeting, Pennsylvania
South Carolina1 site
  • Columbia Dermatology & Aesthetics
    Columbia, South Carolina
    803-731-9600
Tennessee1 site
  • DelRicht Research - Thompson's Station
    Smyrna, Tennessee
    629-895-1775
Texas6 sites
  • Bellaire Dermatology Associates
    Bellaire, Texas
    713-661-4383
  • Modern Research Associates, PLLC
    Dallas, Texas
    214-361-2008
  • Center for Clinical Studies
    Houston, Texas
    713-528-8818
  • Austin Institute for Clinical Research
    Pflugerville, Texas
    512-279-2545
  • Texas Dermatology and Laser Specialists
    San Antonio, Texas
    210-852-2779
  • Center for Clinical Studies
    Webster, Texas
    281-333-2288
Utah1 site
  • Tanner Clinic
    Layton, Utah
Washington2 sites
  • Bellevue Dermatology Clinic
    Bellevue, Washington
    425-455-2275
  • Dermatology of Seattle
    Burien, Washington
    206-248-5020

Timeline

Started enrolling: 2025-03-19. Expected completion: 2028-05. Last updated on ClinicalTrials.gov: 2026-05-14.

Official source

We sync this data quarterly from ClinicalTrials.gov, the federal registry for clinical research. Before contacting a site, verify the trial is still recruiting on the official page:

View on ClinicalTrials.gov →

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