RecruitingNCT07243782

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


Sponsor

Novartis Pharmaceuticals

Enrollment

76 participants

Start Date

Dec 22, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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


Eligibility

Min Age: 6 YearsMax Age: 100 Years

Inclusion Criteria9

  • Hidradenitis suppurativa:
  • 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.
  • Patients who have agreed to participate in study (written informed consent)
  • Pediatric plaque psoriasis:
  • 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.
  • Patients with patient or guardian consent to participate in study (written informed consent)
  • Juvenile idiopathic arthritis:
  • 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.
  • Patients with patient or guardian consent to participate in study (written informed consent)

Exclusion Criteria2

  • Patients who are contraindicated according to national prescribing information
  • Patients participating in other interventional clinical trials

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Interventions

DRUGSecukinumab

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

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NCT07243782


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