Enrolling now · NCT06857942

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

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

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

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

Who can join, in detail

Age 18 and up
Sex All
BMI 27+

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 US sites across 22 states. Contact the site coordinator directly to start the screening process.

Arizona

  • Medical Dermatology Specialists
    Phoenix, Arizona
    602-354-5770

California

  • 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

Florida

  • 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

Georgia

  • Southeast Research Specialists
    Douglasville, Georgia
    678-702-3376

Indiana

  • Dawes Fretzin Clinical Research Group, LLC
    Indianapolis, Indiana
    317-516-5030
  • The Indiana Clinical Trials Center, PC
    Plainfield, Indiana
    317-837-6082

Kentucky

  • Equity Medical - Bowling Green
    Bowling Green, Kentucky
    270-213-7777

Maryland

  • Dermatology and Skin Cancer Specialists, LLC
    Rockville, Maryland

Massachusetts

  • Metro Boston Clinical Partners
    Brighton, Massachusetts

Michigan

  • 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

Nevada

  • Skin Cancer and Dermatology Institute - Reno
    Reno, Nevada
    775-336-3658

New Hampshire

  • Stracskin
    Portsmouth, New Hampshire
    617-833-9995

New Jersey

  • Psoriasis Treatment Center of Central New Jersey
    East Windsor, New Jersey
  • Care Access - Hoboken
    Hoboken, New Jersey
    551-278-8680

New York

  • Equity Medical
    New York, New York
    212-466-6550

North Carolina

  • Revival Research Institute, LLC
    Cary, North Carolina
  • Onsite Clinical Solutions - Huntersville
    Huntersville, North Carolina
    800-785-3150

Ohio

  • Optima Research - Boardman
    Boardman, Ohio
    330-422-3234

Oregon

  • Oregon Dermatology and Research Center
    Portland, Oregon
    503-226-3376

Pennsylvania

  • Dermatology Associates of Plymouth Meeting
    Plymouth Meeting, Pennsylvania

South Carolina

  • Columbia Dermatology & Aesthetics
    Columbia, South Carolina
    803-731-9600

Tennessee

  • DelRicht Research - Thompson's Station
    Smyrna, Tennessee
    629-895-1775

Texas

  • 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

Utah

  • Tanner Clinic
    Layton, Utah

Washington

  • 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:

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