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Terminated Phase 2 Interventional

Efficacy and Safety Study of ABT-436 in Major Depressive Disorder

ClinicalTrials.gov ID: NCT01741142

Public ClinicalTrials.gov record NCT01741142. 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 Jul 22, 2026, 6:42 PM 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 Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of ABT-436 in Major Depressive Disorder

Study identification

NCT ID
NCT01741142
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
19 participants

Conditions and interventions

Interventions

  • ABT-436 Drug
  • Escitalopram 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
Dec 31, 2011
Primary completion
Sep 30, 2013
Completion
Jul 31, 2015
Last update posted
Oct 7, 2013

2012 – 2015

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Site Reference ID/Investigator# 85593 Little Rock Arkansas 72211
Site Reference ID/Investigator# 87228 Garden Grove California 92845
Site Reference ID/Investigator# 87214 National City California 91950
Site Reference ID/Investigator# 87220 Oakland California 94612
Site Reference ID/Investigator# 87215 Bradenton Florida 34201
Site Reference ID/Investigator# 87225 South Miami Florida 33143
Site Reference ID/Investigator# 85594 Atlanta Georgia 30328
Site Reference ID/Investigator# 85580 Marlton New Jersey 08053
Site Reference ID/Investigator# 87227 Brooklyn New York 11235
Site Reference ID/Investigator# 87223 New York New York 10128
Site Reference ID/Investigator# 87217 Dayton Ohio 45417
Site Reference ID/Investigator# 87226 Portland Oregon 97210
Site Reference ID/Investigator# 87221 Philadelphia Pennsylvania 19139
Site Reference ID/Investigator# 87219 Austin Texas 78731
Site Reference ID/Investigator# 87216 Dallas Texas 75231
Site Reference ID/Investigator# 87933 Houston Texas 77008
Site Reference ID/Investigator# 88874 Salt Lake City Utah 84106
Site Reference ID/Investigator# 88876 Seattle Washington 98104

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 NCT01741142, 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 Oct 7, 2013 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01741142 live on ClinicalTrials.gov.

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