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.
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
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 SpecialistsPhoenix, Arizona602-354-5770
California4 sites
- First OC Dermatology Research IncFountain Valley, California714-531-2966
- Center For Dermatology Clinical Research, Inc.Fremont, California510-797-0140
- Metropolis DermatologyLos Angeles, California424-393-0005
- Northridge Clinical TrialsNorthridge, California818-350-7482
Florida5 sites
- NeoClinical ResearchHialeah, Florida305-456-9062
- Skin Care ResearchHollywood, Florida954-674-3535
- Encore Medical ResearchHollywood, Florida954-400-1725
- MOORE Clinical Research, Inc. d/b/a TrueBlue Clinical ResearchTampa, Florida813-948-7550
- TruDerm & TruSpaWellington, Florida
Georgia1 site
- Southeast Research SpecialistsDouglasville, Georgia678-702-3376
Indiana2 sites
- Dawes Fretzin Clinical Research Group, LLCIndianapolis, Indiana317-516-5030
- The Indiana Clinical Trials Center, PCPlainfield, Indiana317-837-6082
Kentucky1 site
- Equity Medical - Bowling GreenBowling Green, Kentucky270-213-7777
Maryland1 site
- Dermatology and Skin Cancer Specialists, LLCRockville, Maryland
Massachusetts1 site
- Metro Boston Clinical PartnersBrighton, Massachusetts
Michigan3 sites
- David Fivenson, MD, PLCAnn Arbor, Michigan734-222-9630
- Great Lakes Research Group, Inc.Bay City, Michigan989-895-9100
- The Derm Institute of West MichiganCaledonia, Michigan616-326-0114
Nevada1 site
- Skin Cancer and Dermatology Institute - RenoReno, Nevada775-336-3658
New Hampshire1 site
- StracskinPortsmouth, New Hampshire617-833-9995
New Jersey2 sites
- Psoriasis Treatment Center of Central New JerseyEast Windsor, New Jersey
- Care Access - HobokenHoboken, New Jersey551-278-8680
New York1 site
- Equity MedicalNew York, New York212-466-6550
North Carolina2 sites
- Revival Research Institute, LLCCary, North Carolina
- Onsite Clinical Solutions - HuntersvilleHuntersville, North Carolina800-785-3150
Ohio1 site
- Optima Research - BoardmanBoardman, Ohio330-422-3234
Oregon1 site
- Oregon Dermatology and Research CenterPortland, Oregon503-226-3376
Pennsylvania1 site
- Dermatology Associates of Plymouth MeetingPlymouth Meeting, Pennsylvania
South Carolina1 site
- Columbia Dermatology & AestheticsColumbia, South Carolina803-731-9600
Tennessee1 site
- DelRicht Research - Thompson's StationSmyrna, Tennessee629-895-1775
Texas6 sites
- Bellaire Dermatology AssociatesBellaire, Texas713-661-4383
- Modern Research Associates, PLLCDallas, Texas214-361-2008
- Center for Clinical StudiesHouston, Texas713-528-8818
- Austin Institute for Clinical ResearchPflugerville, Texas512-279-2545
- Texas Dermatology and Laser SpecialistsSan Antonio, Texas210-852-2779
- Center for Clinical StudiesWebster, Texas281-333-2288
Utah1 site
- Tanner ClinicLayton, Utah
Washington2 sites
- Bellevue Dermatology ClinicBellevue, Washington425-455-2275
- Dermatology of SeattleBurien, Washington206-248-5020
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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