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Clinical Trial Summary

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


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03291067
Study type Interventional
Source Mitsubishi Tanabe Pharma America Inc.
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Status Completed
Phase Phase 2
Start date October 9, 2017
Completion date November 9, 2018