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A 52-week, Multicenter, Randomized, Double-blind, Placebo-controlled Study of Subcutaneous Secukinumab to Demonstrate Efficacy as Assessed by Palmoplantar Pustulosis Psoriasis Area and Severity Index (ppPASI) at 16 Weeks of Treatment, Compared to Placebo, and to Assess Long-term Safety, Tolerability, and Efficacy in Subjects With Moderate to Severe Chronic Palmoplantar Pustular Psoriasis - Amended With an Optional Extension Treatment Period of up to a Total of 148 Weeks

Trial Profile

A 52-week, Multicenter, Randomized, Double-blind, Placebo-controlled Study of Subcutaneous Secukinumab to Demonstrate Efficacy as Assessed by Palmoplantar Pustulosis Psoriasis Area and Severity Index (ppPASI) at 16 Weeks of Treatment, Compared to Placebo, and to Assess Long-term Safety, Tolerability, and Efficacy in Subjects With Moderate to Severe Chronic Palmoplantar Pustular Psoriasis - Amended With an Optional Extension Treatment Period of up to a Total of 148 Weeks

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 18 Mar 2019

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At a glance

  • Drugs Secukinumab (Primary)
  • Indications Pustular psoriasis
  • Focus Registrational; Therapeutic Use
  • Sponsors Novartis
  • Most Recent Events

    • 01 Feb 2019 Primary endpoint (Percentage of Participants With ppPASI 75 Response at Week 16 (Period 1)) has not been met, as per results published in the Journal of the American Academy of Dermatology.
    • 01 Feb 2019 Results published in the Journal of the American Academy of Dermatology
    • 17 Aug 2017 This trial is completed in Belgium (end date: 2017-05-31)
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