drugset / Trial / NCT03093025

A Study to Evaluate the Safety and Efficacy of TS-121 as an Adjunctive Treatment for Major Depressive Disorder

NCT03093025 ↗

Phase 2 Terminated 51 enrolled Taisho Pharmaceutical R&D Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of TS-121 as an adjunctive treatment for patients with major depressive disorder with an inadequate response to current antidepressant Treatment (SSRI, SNRI or bupropion).

Timeline

Start
2017-07-03
Primary completion
2018-11-08
Completion
2018-12-04

Outcome

Outcome not reported

Stopped (Business): “Sponsor decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject BREZIVAPTAN Small molecule 10 mg Oral
Subject BREZIVAPTAN Small molecule 50 mg Oral