Last updated on November 2018

MT-8554 for Reduction of Vasomotor Symptoms in Postmenopausal Women


Brief description of study

The purpose of this study is to assess the efficacy and safety of MT-8554 for treatment of vasomotor symptoms (VMS) associated with menopause.

Detailed Study Description

This is a Phase II randomized, double-blind, placebo-controlled study for dose selection in postmenopausal women with moderate to severe VMS, defined as follows:

  • Moderate: sensation of heat with sweating, able to continue activity
  • Severe: sensation of heat with sweating, causing cessation of activity This study is comprised of a screening period, a run-in period and a 12-week double-blind treatment period.

Clinical Study Identifier: NCT03291067

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Phoenix, AZ United States

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Norfolk, VA United States

Recruitment Status: Closed


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