SEC-HOPE: A Multicenter Retrospective Cohort Study to Estimate Secukinumab Retention Rate in Psoriasis Patients With MASLD
This study aims to examine the retention rate of secukinumab in adult patients with plaque psoriasis (with or without psoriatic arthritis \[PsA\]) and metabolic dysfunction-associated steatotic liver disease (MASLD) in routine clinical practice in Spain, as well as hepatic biomarker trajectories. The study will use electronic medical record (EMR) data from multiple Spanish hospitals.
• Patients with a first recorded secukinumab prescription between 01 January 2021 and 31 December 2023.
• Patients aged ≥18 years at index date.
• Patients with no prior secukinumab exposure in available EMR history.
• Secukinumab must be patient's first-, second-, or third-line biologic therapy for psoriasis/psoriatic arthritis (PsA).
• Patients with documented administration per Summary of Product Characteristics dosing recommendations (SmPC).
• Patients with confirmed plaque psoriasis with or without PsA.
• Patients with at least one cardiometabolic risk factor.
• Patients with a confirmed MASLD diagnosis.
• Patients with baseline laboratory data available.