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Completed Phase 3 Interventional Results available

NVA237 Versus Placebo 12-week Efficacy Study

ClinicalTrials.gov ID: NCT01709864

Public ClinicalTrials.gov record NCT01709864. 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, 11:02 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 12-week Multi-center, Randomized, Double-blind, Placebo Controlled Study to Assess the Efficacy and Safety of NVA237 in Stable COPD Patients

Brief summary

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

The study serves to determine whether the treatment of patients with stable, symptomatic Chronic Obstructive Pulmonary Disease (COPD) with the investigational drug NVA237 is efficient and safe. The efficacy and safety of the drug will be tested against a placebo treatment. The primary criterion to assess efficacy will be the difference between the serial lung function measurements of patients who have been treated for 12 weeks with NVA237 versus those that have received placebo treatment for 12 weeks. A serial lung function measurement (FEV1 testing) will be conducted and the "area under the curve" will be the measure for the ability to breathe.

Study identification

NCT ID
NCT01709864
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
440 participants

Conditions and interventions

Interventions

Drug

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
Oct 31, 2012
Primary completion
Sep 30, 2013
Completion
Sep 30, 2013
Last update posted
Mar 3, 2015

2012 – 2013

United States locations

U.S. sites
54
U.S. states
8
U.S. cities
46
Facility City State ZIP Site status
Novartis Investigative Site Homewood Alabama 35209-6870
Novartis Investigative Site Jasper Alabama 35501
Novartis Investigative Site *See Various Dept.'s* Arizona
Novartis Investigative Site Tucson Arizona 85712
Novartis Investigative Site Fountain Valley California 92708
Novartis Investigative Site Fullerton California 92835
Novartis Investigative Site Los Angeles California 90048
Novartis Investigative Site Los Angeles California 90095
Novartis Investigative Site Riverside California 92506
Novartis Investigative Site San Diego California 92117-4946
Novartis Investigative Site San Diego California 92120
Novartis Investigative Site Brandon Florida 33511
Novartis Investigative Site Clearwater Florida 33756
Novartis Investigative Site DeFuniak Springs Florida 32435
Novartis Investigative Site Edgewater Florida 32132
Novartis Investigative Site Fort Lauderdale Florida 33306
Novartis Investigative Site Hialeah Florida 33012
Novartis Investigative Site Miami Florida 33136
Novartis Investigative Site Miami Florida 33156
Novartis Investigative Site Miami Florida 33173
Novartis Investigative Site Miami Florida 33186
Novartis Investigative Site Pensacola Florida 32503
Novartis Investigative Site Pompano Beach Florida 33060
Novartis Investigative Site Port Orange Florida 32127
Novartis Investigative Site Sarasota Florida 34233
Novartis Investigative Site South Miami Florida 33143
Novartis Investigative Site Summerfield Florida 34491
Novartis Investigative Site Tamarac Florida 33321
Novartis Investigative Site Tampa Florida 33603
Novartis Investigative Site Winter Park Florida 32789
Novartis Investigative Site Las Vegas Nevada 89104
Novartis Investigative Site Las Vegas Nevada 89123
Novartis Investigative Site Charlotte North Carolina 28207
Novartis Investigative Site Raleigh North Carolina 27607
Novartis Investigative Site Shelby North Carolina 28152
Novartis Investigative Site Charleston South Carolina 29406-7108
Novartis Investigative Site Charleston South Carolina 29407
Novartis Investigative Site Columbia South Carolina 29201
Novartis Investigative Site Easley South Carolina 29640
Novartis Investigative Site Gaffney South Carolina 29340
Novartis Investigative Site Greenville South Carolina 29615
Novartis Investigative Site Ninety Six South Carolina 29666
Novartis Investigative Site Rock Hll South Carolina 29732
Novartis Investigative Site Seneca South Carolina 29678
Novartis Investigative Site Simpsonville South Carolina 29681
Novartis Investigative Site Spartanburg South Carolina 29303
Novartis Investigative Site Union South Carolina 29379
Novartis Investigative Site Amarillo Texas 79106-4165
Novartis Investigative Site Arlington Texas 76012
Novartis Investigative Site Arlington Texas 76014
Novartis Investigative Site Beaumont Texas 77701
Novartis Investigative Site Dallas Texas 75251
Novartis Investigative Site Huntsville Texas 77340
Novartis Investigative Site Waco Texas 76712

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 NCT01709864, 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, 2015 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01709864 live on ClinicalTrials.gov.

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