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A randomized, double-blind, multicenter study to assess the efficacy and safety of 16 weeks secukinumab dosage interval shortening (2-weekly 300 mg s.c.) in comparison to continued standard treatment (4-weekly 300 mg s.c.) in patients with moderate-severe plaque type psoriasis who achieved less than clear or almost clear skin (PASI response ≥75 to PASI<90) after 16 weeks under the standard dose of secukinumab

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Trial Profile

A randomized, double-blind, multicenter study to assess the efficacy and safety of 16 weeks secukinumab dosage interval shortening (2-weekly 300 mg s.c.) in comparison to continued standard treatment (4-weekly 300 mg s.c.) in patients with moderate-severe plaque type psoriasis who achieved less than clear or almost clear skin (PASI response ≥75 to PASI<90) after 16 weeks under the standard dose of secukinumab

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Secukinumab (Primary)
  • Indications Plaque psoriasis
  • Focus Registrational; Therapeutic Use
  • Acronyms GAIN
  • Sponsors Novartis

    • Most Recent Events

    • 11 Jul 2020 Primary endpoint (Number of Participants With PASI 90 Response at Week 32) has not been met published in the British Journal of Dermatology
    • 11 Jul 2020 Results published in the British Journal of Dermatology
    • 01 Oct 2016 Status changed from not yet recruiting to completed.

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