drugset / Trial / NCT01724112

Study of the Efficacy and Safety of LY2940094 in Participants With Major Depressive Disorder (MDD)

NCT01724112 ↗

Phase 2 Completed 136 enrolled BlackThorn Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will determine the efficacy, safety, and tolerability of a 40 milligrams (mg) once-daily (QD) dose of LY2940094 for 8 weeks in participants with MDD.

Timeline

Start
2012-11
Primary completion
2014-03
Completion
2014-03

Drugs

EvaluationDrugModalityDoseRoute
Subject LY2940094 Small molecule 40 mg Oral