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RECRUITINGOBSERVATIONAL

Regulatory Post-Marketing Surveillance in Hidradenitis Suppurativa, Pediatric Plaque Psoriasis and JIA Treated With Cosentyx®(Secukinumab) in Korea

Regulatory Post-Marketing Surveillance to Assess Safety and Effectiveness in Hidradenitis Suppurativa, Pediatric Plaque Psoriasis and JIA Treated With Cosentyx®(Secukinumab) in Korea : a rPMS Study

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Regulatory Post-Marketing Surveillance in hidradenitis suppurativa, pediatric plaque psoriasis and JIA treated with Cosentyx®(secukinumab) in Korea

Who May Be Eligible (Plain English)

Who May Qualify: Hidradenitis suppurativa: 1. Adults 18 years of age and older with moderate to severe hidradenitis suppurativa who are or will be receiving Cosentyx within the scope of approved indication. 2. Patients who have agreed to participate in study (written willing to sign a consent form) Pediatric plaque psoriasis: 1. Patients with moderate to severe plaque psoriasis between the ages of 6 and 18 years who are receiving or will receive Cosentyx within the scope of approved indication. 2. Patients with patient or guardian consent to participate in study (written willing to sign a consent form) Juvenile idiopathic arthritis: 1. Enthesitis related arthritis and juvenile psoriatic arthritis in juvenile idiopathic arthritis category patients with enthesitis related arthritis and juvenile psoriatic arthritis in juvenile idiopathic arthritis category between the ages of 6 and 18 years and are receiving or will receive Cosentyx within the scope of approved indication. 2. Patients with patient or guardian consent to participate in study (written willing to sign a consent form) Who Should NOT Join This Trial: 1. Patients who are contraindicated according to national prescribing information 2. Patients participating in other interventional clinical trials Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: Hidradenitis suppurativa: 1. Adults 18 years of age and older with moderate to severe hidradenitis suppurativa who are or will be receiving Cosentyx within the scope of approved indication. 2. Patients who have agreed to participate in study (written informed consent) Pediatric plaque psoriasis: 1. Patients with moderate to severe plaque psoriasis between the ages of 6 and 18 years who are receiving or will receive Cosentyx within the scope of approved indication. 2. Patients with patient or guardian consent to participate in study (written informed consent) Juvenile idiopathic arthritis: 1. Enthesitis related arthritis and juvenile psoriatic arthritis in juvenile idiopathic arthritis category patients with enthesitis related arthritis and juvenile psoriatic arthritis in juvenile idiopathic arthritis category between the ages of 6 and 18 years and are receiving or will receive Cosentyx within the scope of approved indication. 2. Patients with patient or guardian consent to participate in study (written informed consent) Exclusion Criteria: 1. Patients who are contraindicated according to national prescribing information 2. Patients participating in other interventional clinical trials

Treatments Being Tested

DRUG

Secukinumab

This is a prospective observational study. There is no treatment allocation. The decision to initiate treatment will be based solely on clinical judgement.

Locations (1)

Novartis Investigative Site
Seoul, Seoul, South Korea