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Clinical Trial Summary

The primary objective of the study was to assess the long-term safety of 30- and 60-mg daily doses of ospemifene in the treatment of Vulvar and Vaginal Atrophy (VVA) in postmenopausal women with an intact uterus.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01585558
Study type Interventional
Source Shionogi Inc.
Contact
Status Completed
Phase Phase 3
Start date May 16, 2006
Completion date September 18, 2008

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