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NCT Number: NCT07543419

Long Term Observational Study to Collect in a Real-world populatIon Data on the Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe HS Within the Italian Population

The aim of this study is to generate real-world evidence to fill knowledge gaps regarding the response to secukinumab in patients with moderate to severe HS, its treatment patterns, the clinical characteristics of patients on secukinumab, healthcare resource utilization and the economic impact of HS in Italy.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Novartis Investigative Site, Ancona, AN, Italy

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Study participants eligible for inclusion in this study must meet all the following criteria:

  • Male and Female patients who provide written informed consent and privacy form (ICF&PF) to participate in the study.
  • Aged ≥ 18 years at ICF&PF signature. 3. Patients with moderate or severe HS (IHS4 and/or Hurley staging system, as assessed by the investigators) at index date.
  • The start of secukinumab is within 30 days after the ICF&PF signature (enrolment), as per local standard clinical practice. Patients were not treated with secukinumab before enrolment within the Managed Access Program (MAP). The initiation of secukinumab is based on dermatologist's own practice, regardless of study participation.

For HRU and economic burden only:

  • Patients who provide written ICF&PF to allow the use of secondary (administrative) data for the purposes of this study.
  • Patients with more than 12 months of residence inside the area of competence of the LHU (applicable only to study sites associated with the 6 LHUs).

Exclusion criteria

Study participants meeting any of the following criteria are not eligible for inclusion in this study:

  • Participation in an ongoing clinical trial. 8. Any medical or psychological condition that may prevent study participation, based on practitioners' decision-making.

For HRU and economic burden only:

  • Patients will be excluded if the unique identifier does not allow them to be identified in the LHU administrative databases related to the site where they were enrolled.

Treatment and study plan

Primary outcomes

  1. Proportion of patients achieving 55% reduction in IHS4 (IHS4-55) during the observational period.

    Time frame: Baseline,6 months and 1 and 1,5 years after initiation of secukinumab

    Proportion of patients achieving International Hidradenitis Suppurativa Severity Score System 55% reduction(IHS4-55) during the observational period.

    The IHS4 is an exclusively physician-based, clinical scoring system for dynamic assessment of HS severity. Determining IHS4 requires counting nodules, abscesses and draining tunnels/sinus tracts, which is easy to calculate. The IHS4 score is calculated as the number of nodules (multiplied by 1) plus the number of abscesses (multiplied by 2) plus the number of draining tunnels (multiplied by 4). A score of 3 or less signifies mild HS, a score of 4-10 signifies moderate HS and a score of 11 or higher signifies severe HS

Secondary outcomes

  1. Proportion of patients achieving 55% reduction in IHS4 (IHS4-55) stratified by dosing

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    The proportion of patients achieving 55% reduction in IHS4 (IHS4-55) stratified by dosing (q4w / q2w regimen), at 6 months, 1 and 1.5 years after initiation of secukinumab treatment.

    The IHS4 is an exclusively physician-based, clinical scoring system for dynamic assessment of HS severity. Determining IHS4 requires counting nodules, abscesses and draining tunnels/sinus tracts, which is easy to calculate. The IHS4 score is calculated as the number of nodules (multiplied by 1) plus the number of abscesses (multiplied by 2) plus the number of draining tunnels (multiplied by 4). A score of 3 or less signifies mild HS, a score of 4-10 signifies moderate HS and a score of 11 or higher signifies severe HS

  2. Proportion of patients achieving 75% reduction in IHS4 (IHS4-75) and 100% reduction in IHS4 (IHS4-100)

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    The IHS4 is an exclusively physician-based, clinical scoring system for dynamic assessment of HS severity. Determining IHS4 requires counting nodules, abscesses and draining tunnels/sinus tracts, which is easy to calculate. The IHS4 score is calculated as the number of nodules (multiplied by 1) plus the number of abscesses (multiplied by 2) plus the number of draining tunnels (multiplied by 4). A score of 3 or less signifies mild HS, a score of 4-10 signifies moderate HS and a score of 11 or higher signifies severe HS

  3. Proportion of patients achieving 50% reduction in HiSCR (HiSCR-50) and 75% reduction in HiSCR (HiSCR-75)

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    The Hidradenitis Suppurativa Clinical Response (HiSCR) is defined as a ≥ 50% reduction in total AN count (abscesses + inflammatory nodules), and no increase in abscesses or draining tunnels when compared with baseline.

  4. Number, type, and localization of HS lesions

    Time frame: baseline, 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    lesion spread is defined as total abscess and inflammatory nodule count (AN) or draining fistulae in a body region not seen at baseline

  5. Change of total abscess and inflammatory nodule count

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

  6. Proportion of patients receiving up-titration

    Time frame: Within 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Proportion of patients receiving up-titration (q4w-to-q2w) of secukinumab

  7. Proportion of patients receiving down-titration

    Time frame: within 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Proportion of patients receiving down-titration (q2w-to-q4w) of secukinumab

  8. Time to up-titration and down-titration

    Time frame: Up to 1.5 years

    Time to up-titration (q4w-to-q2w) and down-titration (q2w-to-q4w) of secukinumab

  9. Proportion of patients switching from q4w to q2w treatment

    Time frame: 6 months and 1.5 years after initiation of secukinumab treatment

    Proportion of patients switching from q4w to q2w treatment with secukinumab after dose reduction.

  10. Proportion of patients who receive more than one up- and/or down-titration

    Time frame: within 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Proportion of patients who receive more than one up- and/or down-titration of secukinumab

  11. Demographics of adult patients with moderate or severe HS

    Time frame: Baseline

    Descriptive statistics will be performed

  12. Proportion of patients achieving a 5-point reduction of Dermatology life quality index (DLQI) score.

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    The DLQI is a 10-item general dermatology disability index designed to assess health-related quality of life (HRQoL) in adult subjects with skin diseases. The measure is self-administered and includes domains of daily activities, leisure, personal relationships, symptoms and feelings, treatment, and work/school. The recall period is the last week. Each item has four response categories ranging from 0 (not at all) to 3 (very much). "Not relevant" is also a valid response and is scored as 0. The DLQI total score ranges from 0 to 30, with higher scores indicating greater HRQoL impairment

  13. Change in DLQI score from baseline

    Time frame: Baseline, 6 months, 1 and 1.5 years after initiation of secukinumab

    The DLQI is a 10-item general dermatology disability index designed to assess health-related quality of life (HRQoL) in adult subjects with skin diseases. The measure is self-administered and includes domains of daily activities, leisure, personal relationships, symptoms and feelings, treatment, and work/school. The recall period is the last week. Each item has four response categories ranging from 0 (not at all) to 3 (very much). "Not relevant" is also a valid response and is scored as 0. The DLQI total score ranges from 0 to 30, with higher scores indicating greater HRQoL impairment

  14. Clinical characteristics of adult patients with moderate to severe HS

    Time frame: Up to 1.5 years

    Clinical characteristics of adult patients with HS moderate or severe

  15. Proportion of patients with new draining tunnel

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Proportion of patients with new draining tunnel(s) (fistulae/sinuses)

  16. Number of areas affected and proportion of patients with additional area involvement

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

  17. Proportion of patients receiving HS-specific concomitant treatments in combination with secukinumab

    Time frame: Up to 1.5 years

    Proportion of patient as per clinical practice

  18. Time of initiation of concomitant medications

    Time frame: Baseline, 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Time of initiation of concomitant medications (after the initiation of secukinumab)

  19. Duration of treatment with concomitant medications

    Time frame: Up to 1.5 years

    Duration of treatment with concomitant medications in a flexible dosing regimen of secukinumab

  20. Proportion of patients undergoing tapering of concomitant medications

    Time frame: Baseline, 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Proportion of patients undergoing tapering of concomitant medications in a flexible dosing regimen of secukinumab.

  21. Number and type of surgical interventions

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab

    number and type of surgical interventions (minor and major surgical excision; inpatient, outpatient, or self-treatment at home) in a flexible dosing regimen of secukinumab (q4w and q2w)

  22. Reason for surgical intervention

    Time frame: Up to 1.5 years after initiation of secukinumab

  23. Duration of discontinuation/pause of secukinumab treatment before surgery

    Time frame: Up to 1.5 years after initiation of secukinumab

  24. Duration of discontinuation/pause of secukinumab treatment after surgery

    Time frame: Up to 1.5 years after initiation of secukinumab

  25. Reduction in the number of surgical procedures

    Time frame: Up to 1.5 years after initiation of secukinumab

  26. Identification of potential predictors using multivariable analysis

    Time frame: Up to 1.5 years after initiation of secukinumab treatment

  27. Descriptive statistics of pain

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    Descriptive statistics of pain (Numerical Skin Pain Rating Scale).

  28. Proportion of patients achieving a 30% reduction of Pain Numerical Rating scale (NRS30)

    Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment

    The Numerical Skin Pain Rating Scale (NRS) is a scale in which the respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her worst skin pain ranging from 0 (no skin pain) to 10 (skin pain as bad as you can imagine).To assess this, the patient should concentrate on the worst pain that his/her skin lesions has generated during the previous 24 hours.

    NRS30 is a specific threshold used in the assessment of pain reduction in patients with HS. It is defined as a ≥30% and ≥2-point reduction in skin pain on the NRS.

  29. Number of patients with secukinumab AEs in routine clinical practice

    Time frame: Up to 1.5 years after initiation of secukinumab treatment

    Number of patients with secukinumab adverse events (AEs) in routine clinical practice

  30. Hospital Anxiety and Depression Scale [HADS] score

    Time frame: 6 months, 1 and 1.5 years after secukinumab initiation

    The HADS is a widely used screening tool that helps to identify possible or probable instances of anxiety and depression among patients in non-psychiatric hospital settings. It consists of 14 items, with 7 items related to anxiety (HADS-A) and 7 related to depression (HADS-D), collecting how the patient was feeling in the previous week. Each item is scored from 0 to 3, leading to a maximum score of 21 for each subscale. The HADS is beneficial because it excludes somatic symptoms, which might be caused by physical health problems rather than psychological conditions. It is a quick, reliable, and valid measure that can be self-administered, making it a practical tool for clinicians.

  31. Healthcare Resource Utilization of adult patients with HS

    Time frame: 2 months before and 12 months after secukinumab treatment initiation

    describe Healthcare Resource Utilization of adult patients with HS 12 months before and 12 months after secukinumab treatment initiation with administrative claims data

  32. Costs of HS covered by the Italian National Health System

    Time frame: 12 months before and 12 months after secukinumab treatment initiation

    Costs of HS covered by the Italian National Health System (Servizio Sanitario Nazionale, SSN) with administrative Claims data

  33. Direct costs not covered by the SSN and indirect costs of HS

    Time frame: 12 months before and 12 months after secukinumab treatment initiation

    Direct costs not covered by the SSN and indirect costs of HS evaluated through a structured interview between physicians and patients.

  34. Analysis on HS-related surgeries per patient and related direct costs covered by SSN

    Time frame: 12 months after secukinumab treatment initiation

    HS-related surgeries and estimate direct costs of HS-related surgeries covered by the SSN during the period from the date of first HS diagnosis to 12 months after secukinumab treatment initiation with administrative Claims data

Study contacts

Contact information is provided by the study sponsor or research team.

Novartis Pharmaceuticals

CONTACT

[email protected]

+41613241111

Novartis Pharmaceuticals

CONTACT

Sponsors and collaborators

Lead sponsor

Novartis Pharmaceuticals

Industry

Registry information

Official study title

Long Term Observational, Prospective, Multicenter Study to Collect in a Real-world populatIon Data on the Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe Hidradenitis Suppurativa (HS) Within the Italian Population (ANIMA - Italy)

Acronym: ANIMA - Italy

Important dates

Study start
2025
Primary completion
2028
Study completion
2028
First posted
Apr 21, 2026
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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