Regulation of Inflammatory Genes in Hidradenitis Suppurativa
NCT05507125
Bacterial Infections, Bacterial Infections and Mycoses
Birmingham, Alabama, United States
View Trial DetailsNCT Number: NCT07543419
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.
Interested in participating?
Request Info18 year–100 year
All sexes
Observational
Novartis Investigative Site, Ancona, AN, Italy
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:
For HRU and economic burden only:
Exclusion criteria
Study participants meeting any of the following criteria are not eligible for inclusion in this study:
For HRU and economic burden only:
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
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
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
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.
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
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
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
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
Time frame: Up to 1.5 years
Time to up-titration (q4w-to-q2w) and down-titration (q2w-to-q4w) of secukinumab
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.
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
Time frame: Baseline
Descriptive statistics will be performed
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
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
Time frame: Up to 1.5 years
Clinical characteristics of adult patients with HS moderate or severe
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Proportion of patients with new draining tunnel(s) (fistulae/sinuses)
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Time frame: Up to 1.5 years
Proportion of patient as per clinical practice
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)
Time frame: Up to 1.5 years
Duration of treatment with concomitant medications in a flexible dosing regimen of secukinumab
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.
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)
Time frame: Up to 1.5 years after initiation of secukinumab
Time frame: Up to 1.5 years after initiation of secukinumab
Time frame: Up to 1.5 years after initiation of secukinumab
Time frame: Up to 1.5 years after initiation of secukinumab
Time frame: Up to 1.5 years after initiation of secukinumab treatment
Time frame: 6 months, 1 and 1.5 years after initiation of secukinumab treatment
Descriptive statistics of pain (Numerical Skin Pain Rating Scale).
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.
Time frame: Up to 1.5 years after initiation of secukinumab treatment
Number of patients with secukinumab adverse events (AEs) in routine clinical practice
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.
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
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
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.
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
Contact information is provided by the study sponsor or research team.
Novartis Pharmaceuticals
Industry
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
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.
Published trials that share one or more normalized conditions with this study.
NCT05507125
Bacterial Infections, Bacterial Infections and Mycoses
Birmingham, Alabama, United States
View Trial DetailsNCT05403710
Bacterial Infections, Bacterial Infections and Mycoses
Worcester, Massachusetts, United States
View Trial DetailsNCT07049575
Bacterial Infections, Bacterial Infections and Mycoses
Phoenix, Arizona, United States
View Trial DetailsNCT05889182
Bacterial Infections, Bacterial Infections and Mycoses
Birmingham, Alabama, United States
View Trial Details