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A Phase IIa, Double-Blind, Placebo-Controlled, Study of ESN364 Administered for 12 Weeks to Evaluate Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics in Women Presenting With Uterine Fibroids

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Trial Profile

A Phase IIa, Double-Blind, Placebo-Controlled, Study of ESN364 Administered for 12 Weeks to Evaluate Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics in Women Presenting With Uterine Fibroids

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 10 Mar 2017

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At a glance

  • Drugs Fezolinetant (Primary)
  • Indications Uterine leiomyoma
  • Focus Therapeutic Use
  • Sponsors Ogeda
  • Most Recent Events

    • 10 Mar 2017 This trial was completed in Austria(End date: 05 Dec 2016).
    • 26 Feb 2017 This trial was completed in Belgium and Germany (End date: 05 Dec 2016).
    • 19 Jul 2016 According to an Euroscreen media release, the company has opened an Investigational Drug Application (IND) with the U.S. Food and Drug Administration (FDA) to conduct pivotal efficacy and safety assessments to evaluate ESN364 in Phase II studies for the treatment of menopausal hot flashes, poly cystic ovary syndrome and uterine fibroids.
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