drugset / Trial / NCT00406640

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women

NCT00406640

Phase 3 Completed 595 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedSingle-groupTriple-blindTreatment

Summary

Desvenlafaxine succinate (DVS) is a potent and selective serotonin and norepinephrine reuptake inhibitor (SNRI). This study will investigate the safety, efficacy, and tolerability of DVS SR versus escitalopram in women with major depressive disorder (MDD) who are postmenopausal.

Timeline

Start
2006-12
Primary completion
2008-02
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Desvenlafaxine Other / unclassified 50 mg
Comparator Desvenlafaxine Other / unclassified 100 mg
Comparator Desvenlafaxine Other / unclassified 200 mg
Comparator Escitalopram Small molecule 10 mg
Comparator Escitalopram Small molecule 20 mg