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NCT07454889
A Real-world Study of Patients With Hidradenitis Suppurativa and High Cardiovascular Risk or Established Coronary Plaque Treated With Secukinumab
Conditions: Hidradenitis Suppurativa
Sex: All
Ages: 18 Years – 75 Years
Healthy volunteers: No
Enrollment: 34
Sponsor: Novartis Pharmaceuticals
Summary
The aim of this study is to assess the real-world effects of secukinumab in adult participants with moderate-to-severe Hidradenitis Suppurativa (HS), particularly focusing on its potential impact on coronary atherosclerotic plaque progression or stability. Participants will be enrolled at a single dermatology and cardiology center in Italy and will receive secukinumab as part of their routine clinical care
Eligibility Criteria
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 \
Source: ClinicalTrials.gov (NCT07454889). StuddyBuddy aggregates publicly available trial information.