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Hidradenitis SuppurativaANIMA - ItalyNCT07543419

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

An observational study of Hidradenitis Suppurativa, run by Novartis Pharmaceuticals at 16 sites in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 100 years
Conditions the study is for
Hidradenitis Suppurativa
How many people
250 participants
Where
16 sitesItaly
Study dates
17 Dec 2025to 30 Sep 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population will include male and female adult patients (aged ≥ 18 years) with a diagnosis of moderate or severe HS and initiating treatment with secukinumab according to clinical practice

Who may be able to join

  • Study participants eligible for inclusion in this study must meet all the following criteria:
  • 1. Male and Female patients who provide written informed consent and privacy form (ICF\&PF) to participate in the study.
  • 2. 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.
  • 4. 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:
  • 5. Patients who provide written ICF\&PF to allow the use of secondary (administrative) data for the purposes of this study.
  • 6. 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).

Who cannot join

  • Study participants meeting any of the following criteria are not eligible for inclusion in this study:
  • 7. 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:
  • 9. 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.

Trial locations and contacts

16 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Novartis Pharmaceuticals contact

+41613241111

novartis.email@novartis.com

Novartis Pharmaceuticals contact

16 sites in 1 country

Italy16 sites, 16 recruiting
  • Novartis Investigative Site

    Ancona, AN, 60020

    Recruiting
  • Novartis Investigative Site

    Bari, BA, 70124

    Recruiting
  • Novartis Investigative Site

    Brescia, BS, 25123

    Recruiting
  • Novartis Investigative Site

    Cona, FE, 44124

    Recruiting
  • Novartis Investigative Site

    Florence, FI, 50122

    Recruiting
  • Novartis Investigative Site

    Genova, GE, 16132

    Recruiting
  • Novartis Investigative Site

    Lecce, LE, 73100

    Recruiting
  • Novartis Investigative Site

    Messina, ME, 98125

    Recruiting
  • Novartis Investigative Site

    Milan, MI, 20122

    Recruiting
  • Novartis Investigative Site

    Naples, 80131

    Recruiting
  • Novartis Investigative Site

    Palermo, PA, 90127

    Recruiting
  • Novartis Investigative Site

    Perugia, PG, 06129

    Recruiting
  • Novartis Investigative Site

    Rozzano, MI, 20089

    Recruiting
  • Novartis Investigative Site

    San Donato Milanese, MI, 20097

    Recruiting
  • Novartis Investigative Site

    Trento, TN, 38100

    Recruiting
  • Novartis Investigative Site

    Udine, UD, 33100

    Recruiting

Other trials in Italy

About this study

Official 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)

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.

Keywords
Hidradenitis Suppurativa, HS, secukinumab, NIS, LHUs
Medical subject headings
Hidradenitis Suppurativa

What is being measured

The primary outcome is the main question the study is designed to answer.

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

    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

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

Secondary outcomes (34)
  1. Proportion of patients achieving 55% reduction in IHS4 (IHS4-55) stratified by dosing

    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

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

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

    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

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

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

    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.

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

  4. Number, type, and localization of HS lesions

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

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

  5. Change of total abscess and inflammatory nodule count

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

  6. Proportion of patients receiving up-titration

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

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

  7. Proportion of patients receiving down-titration

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

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

  8. Time to up-titration and down-titration

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

    Measured: Up to 1.5 years

  9. Proportion of patients switching from q4w to q2w treatment

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

    Measured: 6 months and 1.5 years after initiation of secukinumab treatment

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

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

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

  11. Demographics of adult patients with moderate or severe HS

    Descriptive statistics will be performed

    Measured: Baseline

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

    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

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

  13. Change in DLQI score from baseline

    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

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

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

    Clinical characteristics of adult patients with HS moderate or severe

    Measured: Up to 1.5 years

  15. Proportion of patients with new draining tunnel

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

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

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

    Measured: 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

    Proportion of patient as per clinical practice

    Measured: Up to 1.5 years

  18. Time of initiation of concomitant medications

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

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

  19. Duration of treatment with concomitant medications

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

    Measured: Up to 1.5 years

  20. Proportion of patients undergoing tapering of concomitant medications

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

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

  21. Number and type of surgical interventions

    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)

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

  22. Reason for surgical intervention

    Measured: Up to 1.5 years after initiation of secukinumab

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

    Measured: Up to 1.5 years after initiation of secukinumab

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

    Measured: Up to 1.5 years after initiation of secukinumab

  25. Reduction in the number of surgical procedures

    Measured: Up to 1.5 years after initiation of secukinumab

  26. Identification of potential predictors using multivariable analysis

    Measured: Up to 1.5 years after initiation of secukinumab treatment

  27. Descriptive statistics of pain

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

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

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

    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.

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

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

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

    Measured: Up to 1.5 years after initiation of secukinumab treatment

  30. Hospital Anxiety and Depression Scale [HADS] score

    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.

    Measured: 6 months, 1 and 1.5 years after secukinumab initiation

  31. Healthcare Resource Utilization of adult patients with HS

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

    Measured: 2 months before and 12 months after secukinumab treatment initiation

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

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

    Measured: 12 months before and 12 months after secukinumab treatment initiation

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

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

    Measured: 12 months before and 12 months after secukinumab treatment initiation

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

    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

    Measured: 12 months after secukinumab treatment initiation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Apr 2026
  2. Study start17 Dec 2025
  3. Primary completion30 Sep 2028 (estimated)
  4. Study completion30 Sep 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
250 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07543419
Sponsor's protocol ID
CAIN457MIT03
Acronym
ANIMA - Italy
Status last verified
Jul 2026
First submitted
14 Nov 2025
Last updated
20 Jul 2026
Results posted
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Hidradenitis Suppurativa, run by Novartis Pharmaceuticals at 16 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 20 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 16 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Novartis Pharmaceuticals (+41613241111, novartis.email@novartis.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2026.

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