drugset / Trial / NCT00785434

Efficacy and Safety of Escitalopram Doses up to 50mg in Treatment of MDD

NCT00785434

Phase 4 Completed 60 enrolled Community Pharmacology Services Ltd
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This will be an open label study of escitalopram. Patients not responsive to citalopram will be switched directly to escitalopram. Patients will receive escalating doses of escitalopram up to a maximum of 50 mg until they either achieve remission (MADRS \<9) or fail to tolerate the dose.

Timeline

Start
2008-10
Primary completion
2009-12
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Escitalopram Small molecule 50 mg