drugset / Trial / NCT01452373

Dehydroepiandrosterone (DHEA) + Acolbifene Against Vasomotor Symptoms (Hot Flushes) in Postmenopausal Women

NCT01452373

Phase 3 Completed 238 enrolled EndoCeutics Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this Phase III trial is to evaluate the efficacy of oral administration of dehydroepiandrosterone (DHEA) combined with acolbifene (a selective estrogen receptor modulator (SERM)) on vasomotor symptoms (hot flushes) in postmenopausal women.

Timeline

Start
2011-10
Primary completion
2012-12
Completion
2013-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject DHEA Unknown 100 mg Oral
Subject acolbifene Other / unclassified 20 mg Oral

Indications

No indication recorded.