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Mytischi, Russian Federation

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  • Secukinumab Drug Survival, Effectiveness and Tolerability in Pediatric Patients With Psoriasis

    This observational study will be performed at healthcare facilities treating pediatric psoriasis patients. The study population will consist of a representative group of pediatric patients with moderate-to-severe plaque psoriasis for whom routine treatment with secukinumab according to the approved national label is initiated during 4 to 16 weeks Retrospective data collection is planned at patients' inclusion. Prospective data collection will continue during follow-up routine visits until secukinumab discontinuation or maximum duration of follow-up for 104 weeks after index date.

    Phase

    N/A

    Span

    188 weeks

    Sponsor

    Novartis Pharmaceuticals

    Mytishchi

    Recruiting

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