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A Phase 3b, Randomized, Double-blind, Placebo-controlled, 24-week Study to Assess the Efficacy and Safety of Fezolinetant in Menopausal Women Suffering From Moderate to Severe Vasomotor Symptoms (Hot Flashes) and Considered Unsuitable for Hormone Replacement Therapy

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Trial Profile

A Phase 3b, Randomized, Double-blind, Placebo-controlled, 24-week Study to Assess the Efficacy and Safety of Fezolinetant in Menopausal Women Suffering From Moderate to Severe Vasomotor Symptoms (Hot Flashes) and Considered Unsuitable for Hormone Replacement Therapy

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 15 Oct 2024

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At a glance

  • Drugs Fezolinetant (Primary)
  • Indications Hot flashes; Vasomotor symptoms
  • Focus Registrational; Therapeutic Use
  • Acronyms DAYLIGHT
  • Sponsors Astellas Pharma Global Development

    • Most Recent Events

    • 10 Oct 2024 According to Astellas Pharma media release,trial design will be presented during the International Menopause Society (IMS) 19th World Congress on Menopause in Melbourne, Australia, October 19-22.
    • 05 Sep 2024 According to an Astellas Pharma media release, data from this DAYLIGHT study will be presented at 2024 Annual Meeting of The Menopause Society on Thursday, Sept. 12.
    • 29 Nov 2023 According to an Astellas Pharma media release, results from this trial will be presented on Nov 30 at the 15th Congress of the European Society of Gynecology in Amsterdam, The Netherlands (Abstract #12497).

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