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Study of efficacy and safety of secukinumab in pediatric patients with severe plaque psoriasis

Phase 3
Completed
Conditions
Severe Chronic Pediatric Plaque Psoriasis
Registration Number
JPRN-jRCT2080223229
Lead Sponsor
ovartis Pharma K.K.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
All
Target Recruitment
5
Inclusion Criteria

*PASI score of 20 or greater at the time of randomization (Wash-out: Other systemic immunomodulating treatments: 4weeks, Phototherapy: 2weeks, Biological immunomodulating agents: 12weeks)

Exclusion Criteria

*Current forms of psoriasis other than chronic plaque-type psoriasis (for example, pustular, erythrodermic, guttate) at randomization
*Previous use of secukinumab or any drug that targets IL-17 or IL-17 receptor
Other protocol-defined inclusion/exclusion criteria may apply.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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