A Phase III, Randomized, Double-blind, Placebo Controlled Multi-center Study of Subcutaneous Secukinumab (150 mg and 300 mg) in Prefilled Syringe to Demonstrate Efficacy (Including Inhibition of Structural Damage), Safety, and Tolerability up to 2 Years in Subjects With Active Psoriatic Arthritis (FUTURE 5)

Trial Profile

A Phase III, Randomized, Double-blind, Placebo Controlled Multi-center Study of Subcutaneous Secukinumab (150 mg and 300 mg) in Prefilled Syringe to Demonstrate Efficacy (Including Inhibition of Structural Damage), Safety, and Tolerability up to 2 Years in Subjects With Active Psoriatic Arthritis (FUTURE 5)

Active, no longer recruiting
Phase of Trial: Phase III

Latest Information Update: 20 Apr 2017

At a glance

  • Drugs Secukinumab (Primary)
  • Indications Psoriatic arthritis
  • Focus Registrational; Therapeutic Use
  • Acronyms FUTURE5
  • Sponsors Novartis
  • Most Recent Events

    • 25 Feb 2017 This trial has been completed in Denmark.
    • 14 Dec 2016 Status changed from recruiting to active, no longer recruiting.
    • 07 Jun 2016 Time frame for primary efficacy endpoint has been changed from week 0-24 to week 0-16.
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