Heart hope for HS patients: drug may slow artery plaque
NCT ID NCT07454889
First seen Jun 25, 2026 · Last updated Aug 27, 2026 · Updated 5 times
Summary
This study follows 34 adults with moderate-to-severe hidradenitis suppurativa (HS) who are taking secukinumab as part of their routine care. Researchers will use a special CT scan to check if the drug affects the buildup of plaque in the heart arteries over 12 months. The goal is to see if treating HS inflammation might also help keep the heart healthier.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- secukinumab
- What this could lead to
- If successful, this could suggest that treating HS with secukinumab may also help stabilize or prevent heart artery plaque, pointing to broader heart benefits.
- What could go wrong
- This is a small, single-center observational study, not a controlled trial. It cannot prove cause and effect, and results may not apply to all patients.
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.
- Participants
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About 34 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Adult participants diagnosed with moderate-to-severe HS who receive secukinumab as part of their routine clinical care at a single dermatology and cardiology center in Italy.
- Ages
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18 to 75 years
- 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: 1. Adult participants aged ≥18 and ≤75 years. 2. Diagnosis of moderate-to-severe HS (International Hidradenitis Suppurativa Severity Score System \[IHS4\] ≥4). 3. Taking or planning to take secukinumab according to standard of care. 4. Participants eligible for coronary imaging by Photon-Counting Computed Tomography (PCCT) based on at least one of the following: 1. Evidence of coronary atherosclerotic plaque previously identified by imaging and receipt of stable, guideline-directed medical therapy. 2. Clinical indication as determined by a cardiologist. 3. Very high risk of developing cardiovascular diseases according to the Systematic Coronary Risk Evaluation 2 (SCORE2) and Systematic Coronary Risk Evaluation 2 - Older Persons (SCORE2-OP) risk models for moderate risk European regions (score ≥7.5% for participants \<50 years old, score ≥10% for participants 50-69 years old, and score ≥15% for participants ≥70 years old). 5. Signed Informed Consent Form (ICF), obtained from the participant or a legally authorized representative, prior to any study-related activities. Exclusion criteria: 1. Known history of previous Myocardial Infarction (MI), Acute Coronary Syndromes (ACS) or Transient Ischemic Attack (TIA) requiring urgent intervention/hospitalization in the last 6 months prior to enrollment. 2. Use of investigational cardiovascular or anti-inflammatory drugs. 3. Use of any other investigational drugs. 4. Chronic Kidney Disease (estimated Glomerular Filtration Rate \[eGFR\] \<30 mL/min). 5. Contraindications to perform PCCT (including allergies to contrast). 6. Other autoimmune systemic diseases or active neoplastic diseases. 7. Known history of Moderate to severe anemia. 8. Congestive Heart Failure (New York Heart Association \[NYHA\] Class III-IV). 9. Pregnant or lactating women.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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