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Clinical Trial Summary

The purpose of this study is to confirm the efficacy of intravaginal prasterone (DHEA) on symptoms of vulvovaginal atrophy due to menopause and to collect further data on subjects exposed to intravaginal DHEA in order to meet the ICH E1 guideline requirements.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02013544
Study type Interventional
Source EndoCeutics Inc.
Contact
Status Completed
Phase Phase 3
Start date February 2014
Completion date February 2015

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