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Completed Phase 2 Interventional

A Study to Evaluate 3 Different Doses of JNJ-31001074 in the Treatment of Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)

ClinicalTrials.gov ID: NCT00880217

Public ClinicalTrials.gov record NCT00880217. 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 2, 2026, 9:52 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- and Active-Controlled, Parallel-Group, Multicenter Study of 3 Dosages of JNJ-31001074 in the Treatment of Adult Subjects With Attention-Deficit/Hyperactivity Disorder

Brief summary

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

The purpose of this study is to evaluate the efficacy and safety/tolerability of 3 different dosages of JNJ-31001074 compared with placebo in adult patients with attention-deficit/hyperactivity disorder (ADHD).

Study identification

NCT ID
NCT00880217
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
430 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Apr 30, 2009
Primary completion
Dec 31, 2009
Completion
Dec 31, 2009
Last update posted
Mar 3, 2013

2009 – 2010

United States locations

U.S. sites
35
U.S. states
22
U.S. cities
35
Facility City State ZIP Site status
Not listed Little Rock Arkansas
Not listed Lafayette California
Not listed Los Alamitos California
Not listed Santa Ana California
Not listed Wildomar California
Not listed Bradenton Florida
Not listed Jacksonville Florida
Not listed North Miami Florida
Not listed Orlando Florida
Not listed South Miami Florida
Not listed St. Petersburg Florida
Not listed Atlanta Georgia
Not listed Boise Idaho
Not listed Eagle Idaho
Not listed Libertyville Illinois
Not listed Overland Park Kansas
Not listed Prairie Village Kansas
Not listed Rochester Hills Michigan
Not listed Saint Charles Missouri
Not listed Mount Kisco New York
Not listed New York New York
Not listed Raleigh North Carolina
Not listed Dayton Ohio
Not listed Oklahoma City Oklahoma
Not listed Eugene Oregon
Not listed Portland Oregon
Not listed Media Pennsylvania
Not listed Charleston South Carolina
Not listed Memphis Tennessee
Not listed Austin Texas
Not listed Wharton Texas
Not listed Burlington Vermont
Not listed Herndon Virginia
Not listed Seattle Washington
Not listed Middleton Wisconsin

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 NCT00880217, 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 Mar 3, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00880217 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →