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Terminated Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03093025

Public ClinicalTrials.gov record NCT03093025. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 6:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled Study of the Safety and Efficacy of TS-121 as an Adjunctive Treatment for Patients With Major Depressive Disorder With an Inadequate Response to Current Antidepressant Treatment

Study identification

NCT ID
NCT03093025
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Taisho Pharmaceutical R&D Inc.
Industry
Enrollment
51 participants

Conditions and interventions

Interventions

  • TS-121 10 mg Drug
  • TS-121 50 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2, 2017
Primary completion
Nov 7, 2018
Completion
Dec 3, 2018
Last update posted
Jul 13, 2020

2017 – 2018

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Woodland International Research Group Little Rock Arkansas 72211
Woodland Research Northwest Rogers Arkansas 72758
Collaborative Neuroscience Network Garden Grove California 92845
PAREXEL Early Phase Clinical Unit Glendale California 91206
Synergy East Lemon Grove California 91945
NRC Research Institute Orange California 92868
MCB Clinical Research Centers Colorado Springs Colorado 80910
Comprehensive Psychiatric Care Norwich Connecticut 06360
Compass Research Orlando Florida 32806
Atlanta Center for Medical Research Atlanta Georgia 30331
Rush University Medical Center Chicago Illinois 60612
Chicago Research Center Chicago Illinois 60634
Alexian Brothers Behavioral Health Hospital Hoffman Estates Illinois 60169
Boston Clinical Trials Boston Massachusetts 02131
Midwest Research Group - St. Charles Psychiatric Associates Saint Charles Missouri 63304
St. Louis Clinical Trials St Louis Missouri 63141
Hassman Research Institute Berlin New Jersey 08009
Global Medical Institutes Princeton New Jersey 08540
SPRI Clinical Trials Brooklyn New York 11235
Midwest Clinical Research Center Dayton Ohio 45417
IPS Research Company Oklahoma City Oklahoma 73103
Grayline Clinical Drug Trials Wichita Falls Texas 76309

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03093025, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 13, 2020 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03093025 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →