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A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of CNTO 1959, a Human Anti-IL 23 Monoclonal Antibody, Following Subcutaneous Administration in Subjects With Palmoplantar Pustulosis

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Trial Profile

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of CNTO 1959, a Human Anti-IL 23 Monoclonal Antibody, Following Subcutaneous Administration in Subjects With Palmoplantar Pustulosis

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Guselkumab (Primary)
  • Indications Palmoplantar pustulosis
  • Focus Proof of concept; Therapeutic Use
  • Sponsors Janssen Pharmaceutical KK

    • Most Recent Events

    • 12 Aug 2021 Results of pool analysis from phase 2 (NCT01845987) and phase 3 (NCT02641730) of guselkumab, assessing the longitudinal profile of PPPASI score improvement by guselkumab treatment and clinical implications of guselkumab dose, baseline disease severity and smoking on the treatment effect, by using pharmacokinetic and pharmacodynamic modeling, published in the Journal of Clinical Pharmacology.
    • 07 Feb 2018 Primary endpoint (Change from baseline in PPSI total score at Week 16) has been met, according to results published in the JAMA Dermatology.
    • 07 Feb 2018 Results published in the JAMA Dermatology.
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