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Completed Phase 3 Interventional

Attention-Deficit Hyperactivity Disorder (ADHD) Study With Adults

ClinicalTrials.gov ID: NCT00048360

Public ClinicalTrials.gov record NCT00048360. 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 May 5, 2026, 6:20 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

An 8-week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Flexible-Dose Comparison of Extended-Release Bupropion Hydrochloride 300-450 mg/Day to Assess the Efficacy, Safety, and Effects on Health Outcomes in the Treatment of Adults With Attention-Deficit/Hyperactivity Disorder

Study identification

NCT ID
NCT00048360
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
162 participants

Conditions and interventions

Interventions

  • Extended-release bupropion hydrochloride Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 60 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
Sep 30, 2002
Primary completion
May 31, 2003
Completion
May 31, 2003
Last update posted
Feb 11, 2013

2002 – 2003

United States locations

U.S. sites
21
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
GSK Clinical Trials Call Center Phoenix Arizona 85016
GSK Clinical Trials Call Center Chula Vista California 91910
GSK Clinical Trials Call Center Lafayette California 94549
GSK Clinical Trials Call Center Northridge California 91324
GSK Clinical Trials Call Center Spring Valley California 91978
GSK Clinical Trials Call Center West Palm Beach Florida 33407
GSK Clinical Trials Call Center Paducah Kentucky 42003
GSK Clinical Trials Call Center Rockville Maryland 20852
GSK Clinical Trials Call Center Cambridge Massachusetts 02138
GSK Clinical Trials Call Center Worcester Massachusetts 01655
GSK Clinical Trials Call Center Omaha Nebraska 68105
GSK Clinical Trials Call Center Chapel Hill North Carolina 27514
GSK Clinical Trials Call Center Beachwood Ohio 44122
GSK Clinical Trials Call Center Cincinnati Ohio 45267-0559
GSK Clinical Trials Call Center Portland Oregon 97209
GSK Clinical Trials Call Center Bellaire Texas 77401
GSK Clinical Trials Call Center Houston Texas 77007
GSK Clinical Trials Call Center Salt Lake City Utah 84132
GSK Clinical Trials Call Center Burlington Vermont 05405
GSK Clinical Trials Call Center Woodstock Vermont 05091
GSK Clinical Trials Call Center 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 NCT00048360, 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 Feb 11, 2013 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00048360 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →