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Clinical Trial Summary

This is a non-interventional, prospective, multi-center real world setting study, aiming to provide safety and effectiveness data in Chinese pediatric patients with moderate to severe plaque psoriasis treated with Cosentyx® for up to 52 weeks.


Clinical Trial Description

Patients who are about to initiate Cosentyx® or have started Cosentyx® within the last 4 weeks and meet the eligibility criteria will be enrolled. Patients will be followed via routine visits in real clinical practice up to 52 weeks. Data from medical records, including safety and effectiveness information of Cosentyx® (e.g., AE, SAE, physical examinations, laboratory tests, disease assessments, etc.) will be collected at each visit. No additional study visits, examinations, laboratory tests or procedures will be mandated throughout the study. ;


Study Design


Related Conditions & MeSH terms

  • Moderate to Severe Chronic Plaque Psoriasis
  • Psoriasis

NCT number NCT05388916
Study type Observational
Source Novartis
Contact
Status Active, not recruiting
Phase
Start date September 8, 2022
Completion date April 30, 2025

See also
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