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Completed Phase 3 Interventional

Study In Subjects With COPD (Chronic Obstructive Pulmonary Disease)

ClinicalTrials.gov ID: NCT00103922

Public ClinicalTrials.gov record NCT00103922. 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 Oct 20, 2026, 5:34 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, 24-week, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety and Tolerability of ARIFLO® (15mg BID) in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

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

This study was designed to determine if the investigational drug is effective and safe in individuals with COPD (chronic pulmonary disease)

Study identification

NCT ID
NCT00103922
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
600 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
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
Nov 2004 (Type not available)
Primary completion
Jan 2007 (Actual)
Completion
Jan 2007 (Actual)
Last update posted
Oct 28, 2016

2004 – 2007

United States locations

U.S. sites
115
U.S. states
34
U.S. cities
106
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Jasper Alabama 35501 —
GSK Investigational Site Phoenix Arizona 85006 —
GSK Investigational Site Tempe Arizona 85282 —
GSK Investigational Site Berkeley California 94705 —
GSK Investigational Site Carmichael California 95608 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Long Beach California 90806 —
GSK Investigational Site Long Beach California 90822 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Murrieta California 92562 —
GSK Investigational Site Rancho Mirage California 92270 —
GSK Investigational Site Riverside California 92805 —
GSK Investigational Site Sacramento California 95823 —
GSK Investigational Site San Diego California 92103 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site San Jose California 95117 —
GSK Investigational Site Sepulveda California 91343 —
GSK Investigational Site Stockton California 95207 —
GSK Investigational Site Torrance California 90509 —
GSK Investigational Site Vista California 92083 —
GSK Investigational Site Walnut Creek California 94598 —
GSK Investigational Site Boulder Colorado 80304 —
GSK Investigational Site Colorado Springs Colorado 80907 —
GSK Investigational Site Denver Colorado 80230 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site Fort Collins Colorado 80528 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Hartford Connecticut 06105 —
GSK Investigational Site Stamford Connecticut 06902 —
GSK Investigational Site Waterbury Connecticut 06708 —
GSK Investigational Site Aventura Florida 33180 —
GSK Investigational Site Brandon Florida 33511 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Largo Florida 33770 —
GSK Investigational Site Longwood Florida 32779 —
GSK Investigational Site Melbourne Florida 32935 —
GSK Investigational Site Panama City Florida 32405 —
GSK Investigational Site Pensacola Florida 32504 —
GSK Investigational Site Tamarac Florida 33321 —
GSK Investigational Site Tampa Florida 33613 —
GSK Investigational Site West Palm Beach Florida 33409 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Coeur d'Alene Idaho 83814 —
GSK Investigational Site Normal Illinois 61761 —
GSK Investigational Site Evansville Indiana 47710 —
GSK Investigational Site South Bend Indiana 46617 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Madisonville Kentucky 42431 —
GSK Investigational Site Lafayette Louisiana 70503 —
GSK Investigational Site New Orleans Louisiana 70119 —
GSK Investigational Site Slidell Louisiana 70461 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Boston Massachusetts 02135 —
GSK Investigational Site Cadillac Michigan 49601 —
GSK Investigational Site Minneapolis Minnesota 55402 —
GSK Investigational Site Jefferson City Missouri 65109 —
GSK Investigational Site Saint Charles Missouri 63301 —
GSK Investigational Site St Louis Missouri 63122 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Billings Montana 59102 —
GSK Investigational Site Missoula Montana 59808 —
GSK Investigational Site Las Vegas Nevada 89104 —
GSK Investigational Site Cherry Hill New Jersey 08003 —
GSK Investigational Site Bronxville New York 10708 —
GSK Investigational Site Cortland New York 14850 —
GSK Investigational Site Larchmont New York 10538 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Charlotte North Carolina 28207 —
GSK Investigational Site Elizabeth City North Carolina 27909 —
GSK Investigational Site High Point North Carolina 27262 —
GSK Investigational Site Statesville North Carolina 28625 —
GSK Investigational Site Chardon Ohio 44024 —
GSK Investigational Site Columbus Ohio 43215 —
GSK Investigational Site Dayton Ohio 45406 —
GSK Investigational Site Sylvania Ohio 43560 —
GSK Investigational Site Lake Oswego Oregon 97035 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Portland Oregon 97213 —
GSK Investigational Site Allentown Pennsylvania 18103 —
GSK Investigational Site Downington Pennsylvania 19335 —
GSK Investigational Site Elverson Pennsylvania 19520 —
GSK Investigational Site Erie Pennsylvania 16508 —
GSK Investigational Site Pittsburgh Pennsylvania 15213 —
GSK Investigational Site Pittsburgh Pennsylvania 15218 —
GSK Investigational Site Pittsburgh Pennsylvania 15243 —
GSK Investigational Site Swarthmore Pennsylvania 19081 —
GSK Investigational Site East Providence Rhode Island 02914 —
GSK Investigational Site Charleston South Carolina 29406-7108 —
GSK Investigational Site Gaffney South Carolina 29340 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Simpsonville South Carolina 29681 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Chattanooga Tennessee 37403 —
GSK Investigational Site Johnson City Tennessee 37601 —
GSK Investigational Site Knoxville Tennessee 37920 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site San Antonio Texas 78205 —
GSK Investigational Site San Antonio Texas 78217 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Salt Lake City Utah 84102 —
GSK Investigational Site Richmond Virginia 23225 —
GSK Investigational Site Richmond Virginia 23229 —
GSK Investigational Site Bellingham Washington 98225 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Spokane Washington 99207 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Morgantown West Virginia 26505 —
GSK Investigational Site Milwaukee Wisconsin 53209-0996 —

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 NCT00103922, 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 28, 2016 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00103922 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →