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Completed Phase 3 Interventional Results available

Long Term Safety Study of NVA237 vs QAB149 in COPD Patients

ClinicalTrials.gov ID: NCT01697696

Public ClinicalTrials.gov record NCT01697696. 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 17, 2026, 9:50 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 Multi-center, Randomized, Double-blind, 52-week Study to Assess the Safety of NVA237 Compared to QAB149 in Patients With Chronic Obstructive Pulmonary Disease (COPD) Who Have Moderate to Severe Airflow Limitation

Brief summary

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

The purpose of the study is to provide long term safety data of NVA237. This study will assess the safety and tolerability of a single dose strength of NVA237.

Study identification

NCT ID
NCT01697696
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
511 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 2012 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Nov 2014 (Actual)
Last update posted
Mar 16, 2016

2012 – 2014

United States locations

U.S. sites
61
U.S. states
27
U.S. cities
55
Facility City State ZIP Site status
Novartis Investigative Site Gulf Shores Alabama 36547 —
Novartis Investigative Site Mobile Alabama 36608 —
Novartis Investigative Site Tucson Arizona 85712 —
Novartis Investigative Site Riverside California 92506 —
Novartis Investigative Site Fort Collins Colorado 80528 —
Novartis Investigative Site Wheat Ridge Colorado 80033 —
Novartis Investigative Site Glastonbury Connecticut 06033 —
Novartis Investigative Site Stamford Connecticut 06902 —
Novartis Investigative Site Waterbury Connecticut 06708 —
Novartis Investigative Site Clearwater Florida 33765 —
Novartis Investigative Site Hialeah Florida 33016 —
Novartis Investigative Site Miami Florida 33165 —
Novartis Investigative Site Miami Florida 33172 —
Novartis Investigative Site Miami Florida 33175 —
Novartis Investigative Site Oakland Park Florida 33334 —
Novartis Investigative Site Pensacola Florida 32503 —
Novartis Investigative Site Couer D'Alene Idaho 83814 —
Novartis Investigative Site Newburgh Indiana 47630 —
Novartis Investigative Site Topeka Kansas 66606 —
Novartis Investigative Site Florence Kentucky 41042 —
Novartis Investigative Site Madisonville Kentucky 42431 —
Novartis Investigative Site New Orleans Louisiana 70119 —
Novartis Investigative Site Opelousas Louisiana 70570 —
Novartis Investigative Site Biddeford Maine 04005 —
Novartis Investigative Site Worchester Massachusetts 01608 —
Novartis Investigative Site Edina Minnesota 55435 —
Novartis Investigative Site Fridley Minnesota 55432 —
Novartis Investigative Site Minneapolis Minnesota 55402 —
Novartis Investigative Site Minneapolis Minnesota 55407 —
Novartis Investigative Site Fremont Nebraska 68025 —
Novartis Investigative Site Omaha Nebraska 68134 —
Novartis Investigative Site Henderson Nevada 89014 —
Novartis Investigative Site Las Vegas Nevada 89119 —
Novartis Investigative Site Lebanon New Hampshire 03756 —
Novartis Investigative Site Calabash North Carolina 28467 —
Novartis Investigative Site Tabor City North Carolina 28463 —
Novartis Investigative Site Columbus Ohio 43215 —
Novartis Investigative Site Columbus Ohio 43235 —
Novartis Investigative Site Marion Ohio 43302 —
Novartis Investigative Site Zanesville Ohio 43701 —
Novartis Investigative Site Eugene Oregon 97404-3233 —
Novartis Investigative Site Philadelphia Pennsylvania 19140 —
Novartis Investigative Site Warwick Rhode Island 02886 —
Novartis Investigative Site Charleston South Carolina 29412 —
Novartis Investigative Site Columbia South Carolina 29204 —
Novartis Investigative Site Greenville South Carolina 29605 —
Novartis Investigative Site Greer South Carolina 29651 —
Novartis Investigative Site North Myrtle Beach South Carolina 29582 —
Novartis Investigative Site Boerne Texas 78006 —
Novartis Investigative Site El Paso Texas 79902 —
Novartis Investigative Site Houston Texas 77043 —
Novartis Investigative Site Houston Texas 77081 —
Novartis Investigative Site Kingwood Texas 77339 —
Novartis Investigative Site San Antonio Texas 78229 —
Novartis Investigative Site White River Junction Vermont 05009 —
Novartis Investigative Site Burke Virginia 22015 —
Novartis Investigative Site Fredericksburg Virginia 22401 —
Novartis Investigative Site Manassas Virginia 20110 —
Novartis Investigative Site Richmond Virginia 23225 —
Novartis Investigative Site Richmond Virginia 23229 —
Novartis Investigative Site Oregon Wisconsin 53575 —

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 NCT01697696, 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 16, 2016 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01697696 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →