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A Study to Estimate Secukinumab Retention Rate in Psoriasis Patients With MASLD

RecruitingN/A

Sponsor: Novartis Pharmaceuticals

Conditions: Plaque Psoriasis, Metabolic Dysfunction-Associated Steatotic Liver Disease

Countries: Spain

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.

Eligibility overview

Sex: ALL

Age: 18 Years to 100 Years

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion criteria:

* 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.

Exclusion criteria:

* Patients with evidence of MASLD absence.
* Patients with malignant liver disease.
* Patients with a history of liver transplantation.
* Patients with alcohol use disorder.
* Patients with other chronic liver diseases.
* Patients with diseases or treatments which cause thrombocytopenia.
* Patients with decompensated cirrhosis.

Other protocol-defined inclusion/exclusion criteria may apply.

Locations (3)

Badalona, Barcelona, Spain
Madrid, Spain
Málaga, Spain