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Completed Phase 3 Interventional Results available

1-year Study to Assess the Efficacy, Safety, and Tolerability of Glycopyrronium Bromide (NVA237) in Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT00929110

Public ClinicalTrials.gov record NCT00929110. 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 18, 2026, 2:05 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 52-week Treatment, Randomized, Double-blind, Placebo-controlled, With Open-label Tiotropium, Parallel-group Study to Assess the Efficacy, Safety, and Tolerability of Glycopyrronium Bromide (NVA237) in Patients With Chronic Obstructive Pulmonary Disease

Brief summary

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

This study was designed to investigate the 1 year efficacy and safety of the 50 µg once daily (od) dose of glycopyrronium bromide (NVA237) in patients with moderate to severe chronic obstructive pulmonary disease.

Study identification

NCT ID
NCT00929110
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis
Industry
Enrollment
1,066 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
Jun 2009 (Type not available)
Primary completion
Apr 2011 (Actual)
Completion
Apr 2011 (Actual)
Last update posted
Aug 17, 2012

2009 – 2011

United States locations

U.S. sites
75
U.S. states
34
U.S. cities
71
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35249 —
Novartis Investigative Site Mobile Alabama 36608 —
Novartis Investigative Site Montgomery Alabama 36117 —
Novartis Investigator Site Fort Smith Arkansas 72901 —
Novartis Investigator Site Anaheim California 92801 —
Novartis Investigative Site Fullerton California 92835 —
Novartis Investigative Site Lakewood California 90712-151 —
Novartis Investigator Site Los Angeles California 90025 —
Novartis Investigator Site Los Angeles California 90048 —
Novartis Investigator Site Mission Viejo California 92691 —
Novartis Investigator Site Paramount California 90723 —
Novartis Investigator Site Riverside California 92506 —
Novartis Investigative Site Rolling Hills Estates California 90274 —
Novartis Investigator Site San Diego California 92120 —
Novartis Investigator Site Colorado Springs Colorado 80907 —
Novartis Investigative site DeLand Florida 32720 —
Novartis Investigative Site Fort Lauderdale Florida 33316-192 —
Novartis Investigative Site Miami Florida 33186 —
Novartis Investigative Site Miami Beach Florida 33140 —
Novartis Investigative Site Ocala Florida 34471 —
Novartis Investigative Site Panama City Florida 32405 —
Novartis Investigative Site Tampa Florida 33606 —
Novartis Investigator Site Winter Park Florida 32789 —
Novartis Investigative Site Atlanta Georgia 30322 —
Novartis Investigative Site Blue Ridge Georgia 30513 —
Novartis Investigative Site Duluth Georgia 30096 —
Novartis Investigator Site Coeur d'Alene Idaho 83814 —
Novartis Investigator Site Skokie Illinois 60076 —
Novartis Investigator Site New Albany Indiana 47150-3054 —
Novartis Investigator Site Valparaiso Indiana 46383 —
Novartis Investigator Site Council Bluffs Iowa 51503-4658 —
Novartis Investigator Site Iowa City Iowa 52240 —
Novartis Investigator Site Shawnee Kansas 66216-1800 —
Novartis Investigative Center Crescent Springs Kentucky 41017 —
Novartis Investigative Site Crestview Hills Kentucky 41017-542 —
Novartis Investigative Site Hazard Kentucky 41701 —
Novartis Investigative Site Louisville Kentucky 40215 —
Novartis Investigator Site Lafayette Louisiana 70508 —
Novartis Investigator Site Sunset Louisiana 70584 —
Novartis Investigator Site Boys Town Maine 68010 —
Novartis Investigative Site Columbia Maryland 21044 —
Novartis Investigative Site Wheaton Maryland 20902 —
Novartis Investigative Site North Dartmouth Massachusetts 02747 —
Novartis Investigative Site Taunton Massachusetts 02780 —
Novartis Investigator Site Minneapolis Minnesota 55402 —
Novartis Investigator Site St Louis Missouri 63122 —
Novartis Investigator Site Bozeman Montana 59718 —
Novartis Investigator Site Lincoln Nebraska 68510 —
Novartis Investigator Site Omaha Nebraska 68131-2197 —
Novartis Investigator Site Papillion Nebraska 68046 —
Novartis Investigative Site Skillman New Jersey 08558 —
Novartis Investigative Site Endwell New York 13760 —
Novartis Investigative site Charlotte North Carolina 28207 —
Novartis Investigator Site Cincinnati Ohio 45245 —
Novartis Investigator Site Sylvania Ohio 43560 —
Novartis Investigator Site Toledo Ohio 43614 —
Novartis Investigator Site Oklahoma City Oklahoma 73103 —
Novartis Investigator Site Oklahoma City Oklahoma 73112 —
Novartis Investigator Site Medford Oregon 97504-8741 —
Novartis Investigator Site Medford Oregon 97504 —
Novartis Investigator Site Portland Oregon 92713 —
Novartis Investigator Site Portland Oregon 97213 —
Novartis Investigative Site Downingtown Pennsylvania 19335-2620 —
Novartis Investigative Site Philadelphia Pennsylvania 19115 —
Novartis Investigative Site East Providence Rhode Island 02914 —
Novartis Investigative Site Providence Rhode Island 02906 —
Novartis Investigative Site North Charleston South Carolina 29406 —
Novartis Investigator Site Austin Texas 78750 —
Novartis Investigator Site El Paso Texas 79902 —
Novartis Investigator Site New Braunfels Texas 78130-6113 —
Novartis Investigator Site San Antonio Texas 78229 —
Novartis Investigator Site Provo Utah 84604-1584 —
Novartis Investigative Site Charlottesville Virginia 22908 —
Novartis Investigator Site Tacoma Washington 98405-4266 —
Novartis Investigator Site Milwaukee Wisconsin 53209 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00929110, 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 Aug 17, 2012 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00929110 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →