Psoriasis Trial, Recruiting NCT06399432 Sponsor: University Hospitals Cleveland Medical Center Condition: Psoriasis
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Psoriasis Trial, Recruiting

NCT06399432
Recruiting Not Applicable

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:

  • You have been diagnosed with chronic plaque psoriasis for at least 12 months before the screening visit.
  • Your psoriasis is considered moderate to severe, based on at least one of the following measures used by your doctor (confirm with trial site).
  • You have been prescribed (but have not yet started) one of these specific psoriasis medications: Secukinumab, Ixekizumab, Brodalumab, Guselkumab, Risankizumab, or Tildrakizumab — and you are willing to start one of them during the study.
  • Apart from your psoriasis, you are in generally good health, as assessed by the study doctor based on your medical history and a physical check-up.
  • You are considered eligible for a weight loss program, meaning you are in good general health and your body mass index (BMI — a measure of body weight relative to height) is between 25 and 40.

Who may not be able to join:

  • You have a significant history of serious heart disease (such as having had a heart attack, blood clots, or a heart stent), inflammatory bowel disease, or other major uncontrolled health conditions affecting organs such as the lungs, liver, kidneys, or immune system.
  • You have any condition that the study doctor believes would put you at risk by participating.
  • You have another skin or inflammatory condition that might make it hard to assess the psoriasis results accurately.
  • You have ever attempted suicide, or have had a serious psychiatric illness requiring a hospital stay in the last 3 years.
  • You are currently pregnant or breastfeeding.
  • You have already tried and not responded to more than 3 systemic (whole-body) treatments for psoriasis.
  • You have a known allergy to any ingredient in the types of psoriasis medications used in this trial (Anti-IL-17 or Anti-IL-23 therapies).
  • You have had a serious infection (such as pneumonia, hepatitis, or blood poisoning) or been hospitalised for an infection, unless you have been fully recovered for more than 4 weeks before screening.
  • You have a history of ongoing or repeated infections, such as chronic chest infections, recurring urinary tract infections, or open/infected skin wounds or ulcers.
  • You have received a BCG vaccination (a type of tuberculosis vaccine) within the past year.
  • You have HIV, or a condition that weakens your immune system (either from birth or acquired).
  • You have had a substance misuse problem within the past 6 months.
  • You have needed antibiotics for a bacterial infection, or had a significant viral or fungal infection, within the past 4 weeks.
  • You have a current or past history of cancer, with the exception of certain fully treated and cured skin cancers or a specific type of treated cervical condition with no recurrence in the past 5 years (confirm with trial site).
  • You have a known nut allergy.
  • You are currently taking part in a supervised diet program.
  • You have used most psoriasis treatments (including creams, tablets, injections, or light therapy) within 2 weeks before the start of the study — though some limited exceptions apply (confirm with trial site for details).
  • You have taken any experimental drug within 2 weeks before the start of the study.
  • You have had prolonged sun exposure or used tanning beds or other UV light sources.
  • Your psoriasis is currently flaring up or is unstable.

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 20 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Neil Korman, MD, University Hospitals Cleveland Medical Center

Phone: 216-844-7546

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
Not Applicable
Sponsor
University Hospitals Cleveland Medical Center
Registry
ClinicalTrials.gov
Start date
18 October 2022
Est. completion
1 July 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Percentage of participants who had a change in blood monocytes profiles.; Percentage of participants who had a change in T-cell profiles.; Change in blood monocyte profile.; Change in T-cell profiles.

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: 20 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