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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 Oct 28, 2026, 8:29 PM 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

Brief summary

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

A study to assess the safety, tolerability and efficacy of NVA237 versus placebo in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD).

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

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 2009 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2010 (Actual)
Last update posted
Apr 12, 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 12, 2012 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01005901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →