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Completed Phase 3 Interventional Results available

Effect of QVA149 Versus NVA237 and Tiotropium on Chronic Obstructive Pulmonary Disorder (COPD) Exacerbations

ClinicalTrials.gov ID: NCT01120691

Public ClinicalTrials.gov record NCT01120691. 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 21, 2026, 1:09 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 64-week Treatment, Multi-center, Randomized, Double-blind, Parallel-group, Active Controlled Study to Evaluate the Effect of QVA149 (110/50 μg o.d.) vs NVA237 (50 μg o.d.) and Open-label Tiotropium (18 μg o.d.) on COPD Exacerbations in Patients With Severe to Very Severe Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

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

This study is designed to assess the effect of once-daily QVA149 on COPD exacerbations in patients with severe to very severe COPD.

Study identification

NCT ID
NCT01120691
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
2,224 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
Apr 2010 (Type not available)
Primary completion
Jul 2012 (Actual)
Completion
Jul 2012 (Actual)
Last update posted
Dec 2, 2013

2010 – 2012

United States locations

U.S. sites
53
U.S. states
25
U.S. cities
49
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35233 —
Novartis Investigative Site Fairhope Alabama 36532 —
Novartis Investigative Site Florence Alabama 35630 —
Novartis Investigative Site Homewood Alabama 35209-6870 —
Novartis Investigative Site Jasper Alabama 35501 —
Novartis Investigative Site Pine Bluff Arkansas 71603 —
Novartis Investigative Site Fullerton California 92835 —
Novartis Investigative Site Palo Alto California 94304-1207 —
Novartis Investigative Site Riverside California 92506 —
Novartis Investigative Site San Diego California 92101 —
Novartis Investigative Site San Diego California 92103-8415 —
Novartis Investigative Site San Diego California 92120 —
Novartis Investigative Site Stockton California 95207 —
Novartis Investigative Site Gainesville Florida 32608 —
Novartis Investigative Site Miami Florida 33125 —
Novartis Investigative Site Pensacola Florida 32503 —
Novartis Investigative Site Couer D'Alene Idaho 83814 —
Novartis Investigative Site Normal Illinois 61761 —
Novartis Investigative Site River Forest Illinois 60305 —
Novartis Investigative Site Florence Kentucky 41042 —
Novartis Investigative Site Louisville Kentucky 40206 —
Novartis Investigative Site Opelousas Louisiana 70570 —
Novartis Investigative Site Bangor Maine 04401 —
Novartis Investigative Site Fridley Minnesota 55432 —
Novartis Investigative Site Ozark Missouri 65721 —
Novartis Investigative Site Saint Charles Missouri 63301 —
Novartis Investigative Site St Louis Missouri 63141 —
Novartis Investigative Site Missoula Montana 59804 —
Novartis Investigative Site Papillion Nebraska 68046 —
Novartis Investigative Site Henderson Nevada 89014 —
Novartis Investigative Site Las Vegas Nevada 89119 —
Novartis Investigative Site Reno Nevada 89520 —
Novartis Investigative Site Great Neck New York 11021 —
Novartis Investigative Site Massapequa New York 11758 —
Novartis Investigative Site Charlotte North Carolina 28207 —
Novartis Investigative Site Raleigh North Carolina 27607 —
Novartis Investigative Site Wilmington North Carolina 28401 —
Novartis Investigative Site Columbus Ohio 43213 —
Novartis Investigative Site Medford Oregon 97504-8741 —
Novartis Investigative Site Portland Oregon 97213 —
Novartis Investigative Site Beaver Pennsylvania 15009 —
Novartis Investigative Site Erie Pennsylvania 16508 —
Novartis Investigative Site Pittsburgh Pennsylvania 15243 —
Novartis Investigative Site Charleston South Carolina 29406-7108 —
Novartis Investigative Site Spartanburg South Carolina 29303 —
Novartis Investigative Site Dallas Texas 75216 —
Novartis Investigative Site Dallas Texas 75246 —
Novartis Investigative Site Fort Worth Texas 76104 —
Novartis Investigative Site Fort Worth Texas 76107 —
Novartis Investigative Site Salt Lake City Utah 84107 —
Novartis Investigative Site Salem Virginia 24153 —
Novartis Investigative Site Tacoma Washington 98405 —
Novartis Investigative Site Green Bay Wisconsin 54311 —

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 289 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01120691, 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 Dec 2, 2013 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01120691 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →