A Randomized, Double-blind, Placebo-controlled Phase III Study of Subcutaneous Secukinumab in Prefilled Syringes to Demonstrate Efficacy at 16 Weeks and to Assess Long-term Efficacy, Safety and Tolerability up to 5 Years in Patients With Active Ankylosing Spondylitis

Trial Profile

A Randomized, Double-blind, Placebo-controlled Phase III Study of Subcutaneous Secukinumab in Prefilled Syringes to Demonstrate Efficacy at 16 Weeks and to Assess Long-term Efficacy, Safety and Tolerability up to 5 Years in Patients With Active Ankylosing Spondylitis

Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 16 Aug 2018

At a glance

  • Drugs Secukinumab (Primary)
  • Indications Ankylosing spondylitis
  • Focus Registrational; Therapeutic Use
  • Acronyms MEASURE 2
  • Sponsors Novartis; Novartis Pharma A.G.; Novartis Pharmaceuticals
  • Most Recent Events

    • 08 Aug 2018 This trial has been completed in Czech Republic, according to European Clinical Trials Database.
    • 16 Jun 2018 Results of pooled data from three phase 3 trials (MEASURE 1-3 [NCT01358175, NCT01649375, NCT02008916]) and from post-marketing analyses, were presented at the 19th Annual Congress of the European League Against Rheumatism.
    • 16 Jun 2018 Results of pooled data from psoriatic arthritis (FUTURE 1-3 studies, n=1414) and ankylosing spondylitis (MEASURE 1-4 studies, n=1163) exposed to SEC was evaluated at baseline and at Week 12, 16 (AS only), 24 and 52, were presented at the 19th Annual Congress of the European League Against Rheumatism.
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