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A Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase III Multicenter Study of Intravenous Secukinumab to Compare Efficacy at 16 Weeks With Placebo and to Assess Safety and Tolerability up to 52 Weeks in Subjects With Active Psoriatic Arthritis

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Trial Profile

A Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase III Multicenter Study of Intravenous Secukinumab to Compare Efficacy at 16 Weeks With Placebo and to Assess Safety and Tolerability up to 52 Weeks in Subjects With Active Psoriatic Arthritis

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 18 May 2025

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At a glance

  • Drugs Secukinumab (Primary)
  • Indications Psoriatic arthritis
  • Focus Registrational; Therapeutic Use
  • Acronyms INVIGORATE 2
  • Sponsors Novartis Pharmaceuticals

Most Recent Events

  • 15 Nov 2023 Results assessing long-term efficacy, safety, and tolerability of intravenous secukinumab in patients with active psoriatic arthritis through 52 weeks, presented at the ACR Convergence 2023.
  • 19 Jul 2022 Status changed from recruiting to completed.
  • 02 Dec 2021 Planned primary completion date changed from 14 Jul 2021 to 18 May 2022.

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