Evaluation of the Effectiveness of Secukinumab in Patients With Moderate to Severe Plaque Psoriasis
Completed
Conditions studied: Plaque Psoriasis
In brief
This study was a real-life study which was based on secondary data collection from the electronic or paper medical records from the Dermatology Clinics of the 14 University, Training \& Research Hospitals in Turkey. Data were extracted between 02 September 2020 and 29 April 2021.
Key facts
- Study ID
- NCT05344482
- Run by
- Novartis Pharmaceuticals
- People needed
- 277
- Starts
- 2020-07-09
- Expected to finish
- 2021-08-31
- Last updated by the study team
- 2022-07-01
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- A diagnosis of psoriasis
- Age ≥ 18 years at registry baseline.
- Patients with a firm diagnosis of chronic plaque psoriasis for at least 6 months before enrollment
- Secukinumab treatment should be initiated 52 weeks before data collection date
- Moderate to severe plaque psoriasis with PASI score of ≥10 before initiating secukinumab.
You may not qualify if…
- Patients diagnosed with others types of psoriasis (pustular psoriasis, erythrodermic psoriasis etc) are excluded.
- Previous exposure to secukinumab or any other biologic drug directly targeting IL-17A or IL-17RA
Where it is running
- Novartis Investigative Site — East Hanover, New Jersey, United States
Full record on ClinicalTrials.gov
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