A Study of Early Secukinumab Treatment in Moderate to Severe Hidradenitis Suppurativa Patients
Starting soon
Conditions studied: Hidradenitis Suppurativa
In brief
The aim of this study is to evaluate the effectiveness of early treatment with secukinumab in patients with moderate-to-severe hidradenitis suppurativa (HS) and assess its impact on disease progression using data from multiple European data sources. All data will be sourced from existing non-interventional study primary data collection, registries, and hospital cohorts that captured information collected in routine clinical practice, prior to and independent of this study.
Key facts
- Study ID
- NCT07690319
- Run by
- Novartis Pharmaceuticals
- People needed
- 186
- Starts
- 2026-10-15
- Expected to finish
- 2027-03-15
- Last updated by the study team
- 2026-07-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with a documented diagnosis of HS (e.g., International Classification of Diseases, 10th Revision [ICD-10] code L73.2);
- Age ≥18 years at index date;
- Moderate-to-severe HS as per label;
- Initiation of secukinumab treatment on or after the first HS diagnosis date;
- And at least one follow-up assessment at 6 or 12 months after index date.
You may not qualify if…
- Patients who had major HS-related surgery (Skin-tissue-sparing Excision with Electrosurgical Peeling [STEEP] or wide excision) in the 12 months prior to index date;
- Patients participating in interventional clinical trials at index date.
- Other protocol-defined inclusion/exclusion criteria may apply.
Full record on ClinicalTrials.gov
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