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Completed Phase 3 Interventional Results available

A Study to Assess the Safety, Tolerability and Efficacy of NVA237 Versus Placebo

ClinicalTrials.gov ID: NCT01005901

Public ClinicalTrials.gov record NCT01005901. 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 Jul 23, 2026, 6:08 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 26-week Treatment, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of NVA237 in Patients With Chronic Obstructive Pulmonary Disease

Study identification

NCT ID
NCT01005901
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis
Industry
Enrollment
1,324 participants

Conditions and interventions

Interventions

  • Glycopyrronium bromide Drug
  • Placebo Drug

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
Sep 30, 2009
Primary completion
Nov 30, 2010
Completion
Nov 30, 2010
Last update posted
Apr 11, 2012

2009 – 2010

United States locations

U.S. sites
33
U.S. states
24
U.S. cities
33
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama
Novartis Investigative Site Fairhope Alabama
Novartis Investigative Site Glendale Arizona
Novartis Investigative Site Los Angeles California
Novartis Investigative Site Walnut Creek California
Novartis Investigative Site Newark Delaware
Novartis Investigative Site Port Orange Florida
Novartis Investigative Site Tamarac Florida
Novartis Investigative Site Topeka Kansas
Novartis Investigative Site Madisonville Kentucky
Novartis Investigative Site Slidell Louisiana
Novartis Investigative Site Biddeford Maine
Novartis Investigative Site Pikesville Maryland
Novartis Investigative Site Ann Arbor Michigan
Novartis Investigative Site Livonia Michigan
Novartis Investigative Site Minneapolis Minnesota
Novartis Investigative Site Kansas City Missouri
Novartis Investigative Site Saint Charles Missouri
Novartis Investigative Site Missoula Montana
Novartis Investigative Site Bellevue Nebraska
Novartis Investigative Site Omaha Nebraska
Novartis Investigative Site Reno Nevada
Novartis Investigative Site New Brunswick New Jersey
Novartis Investigative Site Rochester New York
Novartis Investigative Site Cincinnati Ohio
Novartis Investigative Site Oklahoma City Oklahoma
Novartis Investigative Site Tulsa Oklahoma
Novartis Investigative Site Lincoln Rhode Island
Novartis Investigative Site Johnson City Tennessee
Novartis Investigative Site Corpus Christi Texas
Novartis Investigative Site McKinney Texas
Novartis Investigative Site San Antonio Texas
Novartis Investigative Site Richmond Virginia

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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01005901, 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 Apr 11, 2012 · Synced Jul 23, 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 protocol, eligibility criteria, and contact information for NCT01005901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →