Could an antibody fight both psoriasis and heart disease?
NCT ID NCT04776629
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This phase 2 trial tested a drug called orticumab in 77 adults with moderate-to-severe psoriasis who also had cardiometabolic risks (like obesity and high cholesterol). The goal was to see if orticumab could safely reduce skin plaques and inflammation linked to heart disease. Participants received either the drug or a placebo, and researchers measured changes in psoriasis severity and other health markers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- orticumab (a lab-made antibody targeting oxidized LDL)
- What this could lead to
- If it works, this could point toward a treatment that helps both psoriasis skin symptoms and related heart disease risks.
- What could go wrong
- This is a small, early-phase proof-of-activity study, not a large confirmatory trial. The drug may not improve psoriasis or heart markers, and side effects are still being evaluated.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
77 people
The number who actually took part.
- Started
-
Jun 2021
- Finished
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Nov 2022
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
30 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Stable/chronic plaque psoriasis with PASI score of ≥ 12 AND involving ≥ 10% of the subject's BSA.- ≥ 30 years of age at time of consent. * BMI ≥ 30 kg/m2 * LDL ≥ 100 mg/dL at Screening. * All females must have a negative serum pregnancy test result at Screening and a negative urine pregnancy test prior to dosing. Exclusion Criteria: Subjects are excluded from the study if any of the following criteria are met: * Past use of orticumab. * Any of the nonplaque forms of psoriasis: erythrodermic, guttate, or pustular. * Scalp, palmar or plantar psoriasis only, at Screening or Baseline. * Have evidence of skin conditions (e.g., eczema) at the time of Screening or Baseline visit that would interfere with theevaluation of psoriasis. * Newly discovered Type 2 diabetes mellitus (T2DM) * Moderate or high-intensity statin use or new use of a low-intensity statin therapy. * No use of anti-coagulating or anti-thrombotic agents. * Poorly controlled hypertension * Use of an IL-23 blocker in the past 180 days, an IL-17 blocker in the past 16 weeks, or a TNF blocker in the past 12 weeks. * Use of methotrexate, cyclosporine, or apremilast in the past 4 weeks. * History of hypersensitivity or allergies to any contents in the orticumab formulation. * A history of any clinically important abnormalities in cardiac rhythm or conduction. * A history of prolonged QT intervals or a family history of long QT-syndrome at Screening. * A history of first, second or third-degree atrioventricular (AV) block, or AV dissociation. * A history of complete bundle branch block. * Unstable angina pectoris, myocardial infarction, transient ischemic attack, or stroke within 3 months prior to Screening, or participants who have undergone percutaneous coronary intervention or a coronary artery bypass graft within 6 months prior to Screening or who are due to undergo these procedures at the time of Screening. * Severe congestive heart failure (NYHA III or IV).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Blue Coast Research Center
Vista, California, 92083, United States
-
CCT Research - Springville Dermatology
Springville, Utah, 84663, United States
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CCT- Research at the center for Dermatology and Plastic Surgery
Scottsdale, Arizona, 85260, United States
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Center for Clinical Studies, LTD.LLP
Webster, Texas, 77598, United States
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Dawes Fretzin Clinical Research Group, LLC
Indianapolis, Indiana, 46250, United States
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Derm Institute & Skin Care Ctr., Inc.
Santa Monica, California, 90404, United States
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Excel Clinical Research
Las Vegas, Nevada, 89109, United States
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Jacksonville Center for Clinical Research
Jacksonville, Florida, 32216, United States
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Las Vegas Clinical Trials
Las Vegas, Nevada, 89030, United States
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Orange County Research Center
Tustin, California, 92780, United States
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SMS Clinical Research
Mesquite, Texas, 75149, United States
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Texas Dermatology and Laser Specialists
San Antonio, Texas, 78218, United States
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Vital Prospects Clinical Research Institute, PC
Tulsa, Oklahoma, 85260, United States
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