A Randomized, Double-blind, Double Dummy, Multicenter Study to Assess the Safety, Tolerability and Long-term Efficacy of Intravenous (10mg/kg) and Subcutaneous (300mg) Secukinumab in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis Who Are Partial Responders to Secukinumab [EXTENSION OF 700203953]

Trial Profile

A Randomized, Double-blind, Double Dummy, Multicenter Study to Assess the Safety, Tolerability and Long-term Efficacy of Intravenous (10mg/kg) and Subcutaneous (300mg) Secukinumab in Subjects With Moderate to Severe Chronic Plaque-type Psoriasis Who Are Partial Responders to Secukinumab [EXTENSION OF 700203953]

Completed
Phase of Trial: Phase III

Latest Information Update: 24 Aug 2016

At a glance

  • Drugs Secukinumab (Primary) ; Secukinumab (Primary)
  • Indications Plaque psoriasis
  • Focus Therapeutic Use
  • Acronyms STATURE
  • Sponsors Novartis
  • Most Recent Events

    • 12 May 2016 Results (pooled analysis of this and other nine studies, n = 3993) assessing safety of secukinumab published in the Journal of the American Academy of Dermatology.
    • 06 Oct 2013 Results were presented at the 22nd Congress of the European Association of Dermatology and Venereology (EADV), in October 2013, according to a Novartis media release.
    • 25 Sep 2013 New source identified and integrated (ClinicalTrials.gov: US National Institutes of Health: NCT01412944)
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