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Completed Phase 2 Interventional

A Phase 2 Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizophrenia

ClinicalTrials.gov ID: NCT01678755

Public ClinicalTrials.gov record NCT01678755. 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 Sep 4, 2026, 8:24 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 Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Study of the Safety and Efficacy of ABT-126 in the Treatment of Cognitive Deficits in Schizophrenia (CDS) in Smokers

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is an efficacy study evaluating a experimental treatment for cognitive deficits in adults with schizophrenia.

Study identification

NCT ID
NCT01678755
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
157 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
20 Years to 55 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 31, 2012
Primary completion
Feb 28, 2014
Completion
Feb 28, 2014
Last update posted
Jul 6, 2021

2012 – 2014

United States locations

U.S. sites
20
U.S. states
10
U.S. cities
20
Facility City State ZIP Site status
Site Reference ID/Investigator# 74436 Chino California 91710
Site Reference ID/Investigator# 72704 Garden Grove California 92845
Site Reference ID/Investigator# 72699 National City California 91950
Site Reference ID/Investigator# 73983 Oceanside California 92056
Site Reference ID/Investigator# 73236 Orange California 92868
Site Reference ID/Investigator# 86974 San Diego California 92102
Site Reference ID/Investigator# 72701 Torrance California 90502
Site Reference ID/Investigator# 75314 Bradenton Florida 34201
Site Reference ID/Investigator# 75146 Maitland Florida 32751
Site Reference ID/Investigator# 75654 Atlanta Georgia 30308
Site Reference ID/Investigator# 72703 Chicago Illinois 60640
Site Reference ID/Investigator# 76534 Hoffman Estates Illinois 60169
Site Reference ID/Investigator# 73984 Lake Charles Louisiana 70629
Site Reference ID/Investigator# 73981 St Louis Missouri 63109
Site Reference ID/Investigator# 89553 Marlton New Jersey 08053
Site Reference ID/Investigator# 72700 Cedarhurst New York 11516
Site Reference ID/Investigator# 73982 New York New York 10065
Site Reference ID/Investigator# 113035 Oklahoma City Oklahoma 73116
Site Reference ID/Investigator# 72702 DeSoto Texas 75115
Site Reference ID/Investigator# 75147 Houston Texas 77008

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 NCT01678755, 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 6, 2021 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01678755 live on ClinicalTrials.gov.

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