Characteristics of Patients Treated With Secukinumab for Moderate to Severe Plaque Psoriasis
NCT ID: NCT05650060
Last Updated: 2023-04-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
163 participants
OBSERVATIONAL
2021-01-20
2021-12-23
Brief Summary
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Detailed Description
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At each study site, patients who were treated with secukinumab or had ever been treated with secukinumab for moderate to severe plaque psoriasis were included for screening by chronological order starting from the most recent date (April 2021) to September 2017. This was to include the most recent clinical practice in the study.
The data of patients diagnosed with moderate-to-severe chronic plaque-type psoriasis who received secukinumab in real clinical practice at least 1 dose were collected. The medical records were reviewed to collect the data from the date of the first diagnosis of psoriasis till the most recent dose of secukinumab.
The data of secukinumab use and clinical outcome (PASI score) were collected at 4 and 16 weeks after first dose initiation and at the most recent dose of secukinumab. The total number of secukinumab injections at the 3-time points were collected.
An index date was defined for each patient. The first secukinumab injection observed in the medical records was considered the index date for the exploratory endpoint.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Secukinumab
all patients with psoriasis who received secukinumab
Secukinumab
all patients with psoriasis who received secukinumab
Interventions
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Secukinumab
all patients with psoriasis who received secukinumab
Eligibility Criteria
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Inclusion Criteria
* Previous diagnosis of moderate to severe plaque psoriasis as hospital record with available baseline PASI at index date (date 0 to date -7 prior index date)
* Initiated treatment with secukinumab for moderate to severe plaque psoriasis during September 2017-April 2021
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Novartis Pharmaceuticals
INDUSTRY
Responsible Party
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Principal Investigators
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Novartis Pharmaceuticals
Role: STUDY_DIRECTOR
Novartis Pharmaceuticals
Locations
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Novartis Investigative Site
Bangkok, , Thailand
Countries
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Other Identifiers
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CAIN457ATH01
Identifier Type: -
Identifier Source: org_study_id
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