drugset / Trial / NCT01482221

A Study to Assess the Effect and Safety of AZD6765 in Patients With Major Depressive Disorder

NCT01482221

Phase 2 Completed 542 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the effect and safety of AZD6765 in patients with major depressive disorder who exhibit inadequate response to antidepressants. AZD6765 is a channel blocker of the N-methyl-D-aspartate (NMDA) class of glutamate receptors.

Timeline

Start
2011-12-16
Primary completion
2013-08-26
Completion
2013-08-26

Drugs

EvaluationDrugModalityDoseRoute
Subject lanicemine Small molecule 50 mg Intravenous
Subject lanicemine Small molecule 100 mg Intravenous