Mediterranean Diet vs no Dietary Intervention for Improving Signs and Symptoms of Psoriasis in Patients Treated With Anti-IL-17 or Anti-IL-23 Inhibitors
Launched by UNIVERSITY HOSPITALS CLEVELAND MEDICAL CENTER · Apr 30, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying whether following a Mediterranean diet can help improve the signs and symptoms of psoriasis in patients who are starting treatment with specific medications called Anti-IL-17 or Anti-IL-23 inhibitors. The Mediterranean diet focuses on healthy foods like fruits, vegetables, whole grains, and healthy fats, while the other group will not follow any specific dietary changes. If you have been diagnosed with chronic plaque psoriasis for at least a year and are in good health (aside from psoriasis), you might be eligible to participate. You should also be willing to start one of the mentioned medications during the study.
Participants will have a total of 3 or 4 visits over about 10 weeks. There will be a two-week period when certain psoriasis medications must be paused, but if you’re not using those medications, you can complete your visits in a shorter time frame. Throughout the trial, you will receive guidance on the diet and begin your prescribed psoriasis treatment after following the Mediterranean diet for four weeks. This study aims to see if the diet can make a difference while you are on the new medication.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Diagnosis of chronic plaque psoriasis for at least 12 months prior to Screening.
- • Have moderate to severe plaque psoriasis at Baseline as defined by
- • 1. BSA ≥5% OR
- • 2. sPGA ≥3 (moderate to severe) OR
- • 3. PASI ≥5
- • Must have been prescribed, per standard-of-care, an Anti-IL-17 or Anti-IL-23 therapy for psoriasis, which the patient has not yet started, but is willing to start during the study.
- • Eligible therapies are Secukinumab, Ixekizumab, Brodalumab, Guselkumab, Risankizumab, and Tildrakizumab.
- • Must be in good health (except for psoriasis) as judged by the Investigator, based on medical history and physical examination.
- • Must be eligible for a weight loss program, defined as being in good general health and having a BMI between 25 to 40.
- Exclusion Criteria:
- • Other than psoriasis, history of any clinically significant (as determined by the Investigator) cardiac (clinically advanced cardiovascular disease including stent, past history of MI, thrombotic event or arterial calcification), active or history of inflammatory bowel disease, endocrinologic, pulmonary, neurologic, psychiatric, hepatic, renal, hematologic, immunologic disease, or other major uncontrolled disease.
- • Any condition, including the presence of laboratory abnormalities, which would place the subject at unacceptable risk if he/she were to participate in the study.
- • Any condition, including other inflammatory diseases or dermatologic conditions that confound the ability to interpret data from the study.
- • Prior history of suicide attempt at any time in the subject's lifetime prior to screening or randomization, or major psychiatric illness requiring hospitalization within the last 3 years.
- • Pregnant or breast-feeding.
- • Have failed more than 3 systemic agents for treatment of psoriasis.
- • History of allergy to any component of Anti-IL-17 or Anti-IL-23 therapies.
- • Had a serious infection (including, but not limited to, hepatitis, pneumonia, sepsis, cellulitis, meningitis or pyelonephritis) or have been hospitalized for an infection. Subject must be cured of infection \> 4 weeks before Screening.
- • Have a history of, or ongoing, chronic or recurrent infectious disease, including, but not limited to, chronic renal infection, chronic chest infection (e.g., bronchiectasis), sinusitis, recurrent urinary tract infection (e.g., recurrent pyelonephritis, chronic non-remitting cystitis), an open, draining, or infected skin wound or ulcer.
- • Had a Bacillus Calmette-Guérin (BCG) vaccination within 1 year prior to screening.
- • History of positive human immunodeficiency virus (HIV), or have congenital or acquired immunodeficiency (e.g., common variable immunodeficiency disease).
- • Active substance abuse or a history of substance abuse within 6 months prior to Screening.
- • Bacterial infections requiring treatment with oral or injectable antibiotics, or significant viral or fungal infections, within 4 weeks of Screening. Any treatment and cure for such infections must have been completed at least 4 weeks prior to Screening.
- * Malignancy or history of malignancy, except for:
- • 1. treated \[i.e., cured\] basal cell or squamous cell in situ skin carcinomas;
- • 2. treated \[i.e., cured\] cervical intraepithelial neoplasia \[CIN\] or carcinoma in situ of the cervix with no evidence of recurrence within the previous 5 years.
- • Have a known nut allergy.
- • Currently participating in a supervised dietary program.
- • Use of psoriasis therapy 2 weeks prior to Baseline (including, but not limited to, topical corticosteroids, retinoids or vitamin D analog preparations, tacrolimus, pimecrolimus, anthralin/dithranol, cyclosporine, corticosteroids, methotrexate, retinoids, mycophenolate, thioguanine, hydroxyurea, sirolimus, sulfasalazine, azathioprine, fumaric acid esters, TNF inhibitors IL-17 inhibitors, IL-12/23 inhibitors, or phototherapy).
- • Exceptions: Low-potency corticosteroids will be allowed as background therapy and restricted to treatment of the face, axillae, and groin in accordance with the manufacturers' suggested usage during the course of the study (this restricted usage should be documented). Subjects with scalp psoriasis will be permitted to use coal tar shampoo and/or salicylic acid scalp preparations on scalp lesions. An unmedicated skin moisturizer (e.g. Eucerin®) will be also permitted for body lesions only. Subjects should not use these topical treatments within 24 hours prior to the clinic visit.
- • Use of any investigational drug within 2 weeks prior to Baseline.
- • Prolonged sun exposure or use of tanning booths or other ultraviolet (UV) light sources.
- • Currently flaring or unstable psoriasis.
About University Hospitals Cleveland Medical Center
University Hospitals Cleveland Medical Center is a leading academic medical center renowned for its commitment to advancing healthcare through innovative research and clinical excellence. Affiliated with Case Western Reserve University, the center integrates cutting-edge medical education, comprehensive patient care, and pioneering clinical trials to enhance treatment options and improve patient outcomes. With a diverse range of specialized programs and a robust infrastructure for research, University Hospitals Cleveland Medical Center plays a vital role in translating scientific discoveries into effective therapies, ensuring access to the latest advancements in medicine for patients and communities.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Cleveland, Ohio, United States
Patients applied
Trial Officials
Neil Korman, MD
Principal Investigator
University Hospitals Cleveland Medical Center
Jordan K Kahle, MD
Principal Investigator
University Hospitals Cleveland Medical Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported