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.
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
16 sites in 1 country
Italy16 sites, 16 recruiting
- 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
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.
- Conditions
- Hidradenitis Suppurativa
- 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.
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)
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
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
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
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
Change of total abscess and inflammatory nodule count
Measured: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
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
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
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
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
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
Demographics of adult patients with moderate or severe HS
Descriptive statistics will be performed
Measured: Baseline
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
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
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
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
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
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
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
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
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
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
Reason for surgical intervention
Measured: Up to 1.5 years after initiation of secukinumab
Duration of discontinuation/pause of secukinumab treatment before surgery
Measured: Up to 1.5 years after initiation of secukinumab
Duration of discontinuation/pause of secukinumab treatment after surgery
Measured: Up to 1.5 years after initiation of secukinumab
Reduction in the number of surgical procedures
Measured: Up to 1.5 years after initiation of secukinumab
Identification of potential predictors using multivariable analysis
Measured: Up to 1.5 years after initiation of secukinumab treatment
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
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
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
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
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
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
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
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.
- First posted21 Apr 2026
- Study start17 Dec 2025
- Primary completion30 Sep 2028 (estimated)
- Study completion30 Sep 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hidradenitis SuppurativaStudies of the same condition, open and under way.
- More trials run by Novartis PharmaceuticalsThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Novartis Pharmaceuticals, Study director, Novartis Pharmaceuticals
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
Study at a glance
From the registry record, last updated by the sponsor on 20 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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)
- ClinicalTrials.gov ID
- NCT07543419
- Acronym / sponsor ID
- ANIMA - Italy / CAIN457MIT03
- Conditions
- Hidradenitis Suppurativa
- Keywords
- Hidradenitis Suppurativa, HS, secukinumab, NIS, LHUs
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 250 participants (estimated)
- Lead sponsor
- Novartis PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- 17 Dec 2025 (actual)
- Primary completion
- 30 Sep 2028 (estimated)
- Study completion
- 30 Sep 2028 (estimated)
- First posted
- 21 Apr 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Other
Who may qualify
- Ages
- 18 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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
Key inclusion criteria (7 listed)
- 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.
- 5. Patients who provide written ICF\&PF to allow the use of secondary (administrative) data for the purposes of this study.
Key exclusion criteria (4 listed)
- 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.
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
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
34 secondary outcomes
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
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
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
Number, type, and localization of HS lesions
Time frame: baseline, 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Change of total abscess and inflammatory nodule count
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
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 down-titration
Time frame: within 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Time to up-titration and down-titration
Time frame: Up to 1.5 years
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 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
Demographics of adult patients with moderate or severe HS
Time frame: Baseline
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
Change in DLQI score from baseline
Time frame: Baseline, 6 months, 1 and 1.5 years after initiation of secukinumab
Clinical characteristics of adult patients with moderate to severe HS
Time frame: Up to 1.5 years
Proportion of patients with new draining tunnel
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
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
Proportion of patients receiving HS-specific concomitant treatments in combination with secukinumab
Time frame: Up to 1.5 years
Time of initiation of concomitant medications
Time frame: Baseline, 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Duration of treatment with concomitant medications
Time frame: Up to 1.5 years
Proportion of patients undergoing tapering of concomitant medications
Time frame: Baseline, 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Number and type of surgical interventions
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab
Reason for surgical intervention
Time frame: Up to 1.5 years after initiation of secukinumab
Duration of discontinuation/pause of secukinumab treatment before surgery
Time frame: Up to 1.5 years after initiation of secukinumab
Duration of discontinuation/pause of secukinumab treatment after surgery
Time frame: Up to 1.5 years after initiation of secukinumab
Reduction in the number of surgical procedures
Time frame: Up to 1.5 years after initiation of secukinumab
Identification of potential predictors using multivariable analysis
Time frame: Up to 1.5 years after initiation of secukinumab treatment
Descriptive statistics of pain
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
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
Number of patients with secukinumab AEs in routine clinical practice
Time frame: Up to 1.5 years after initiation of secukinumab treatment
Hospital Anxiety and Depression Scale [HADS] score
Time frame: 6 months, 1 and 1.5 years after secukinumab initiation
Healthcare Resource Utilization of adult patients with HS
Time frame: 2 months before and 12 months after secukinumab treatment initiation
Costs of HS covered by the Italian National Health System
Time frame: 12 months before and 12 months after secukinumab treatment initiation
Direct costs not covered by the SSN and indirect costs of HS
Time frame: 12 months before and 12 months after secukinumab treatment initiation
Analysis on HS-related surgeries per patient and related direct costs covered by SSN
Time frame: 12 months after secukinumab treatment initiation
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Novartis Pharmaceuticals contact
Novartis Pharmaceuticals study director
Novartis Pharmaceuticals
16 sites in 1 country: see every site and its status.
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.