drugset / Trial / NCT01586364

Long-Term Safety of Ospemifene 60 mg Oral Daily Dose for the Treatment of Vulvar and Vaginal Atrophy (VVA) in Postmenopausal Women Without a Uterus

NCT01586364

Phase 3 Completed 301 enrolled Shionogi QuatRx Pharmaceuticals · collab
NaSingle-groupOpen-labelTreatment

Summary

The objective of the study was to assess the long-term safety of daily doses of ospemifene 60 mg in the treatment of vulvar and vaginal atrophy (VVA) in postmenopausal women without a uterus.

Timeline

Start
2006-05-08
Primary completion
2008-11-21
Completion
2008-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Ospemifene Other / unclassified 60 mg Oral

Indications