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Completed Phase 3 Interventional Results available

12-week Efficacy of Indacaterol

ClinicalTrials.gov ID: NCT01072448

Public ClinicalTrials.gov record NCT01072448. 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, 10:24 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 Treatment, Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Assess the Efficacy and Safety of Once Daily Indacaterol in Patients With Chronic Obstructive Pulmonary Disease

Brief summary

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

This 12-week study evaluated the efficacy and safety of indacaterol versus placebo.

Study identification

NCT ID
NCT01072448
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis
Industry
Enrollment
323 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
Dec 31, 2009
Primary completion
Jun 30, 2010
Completion
Jun 30, 2010
Last update posted
Aug 18, 2011

2010

United States locations

U.S. sites
62
U.S. states
29
U.S. cities
60
Facility City State ZIP Site status
Novartis Investigator Site Peoria Arizona 85381
Novartis Investigator Site Pine Bluff Arkansas 71603
Novartis Investigator Site Buena Park California 90620
Novartis Investigator Site Encinitas California 92024
Novartis Investigator Site Fountain Valley California 92708
Novartis Investigator Site Los Angeles California 90015
Novartis Investigator Site San Diego California 92103
Novartis Investigator Site San Diego California 92120
Novartis Investigator Site Temecula California 92591
Novartis Investigator Site Torrance California 90505
Novartis Investigator Site Walnut Creek California 94598
Novartis Investigator Site Wheat Ridge Colorado 80033
Novartis Investigative Site Port Orange Florida 32127
Novartis Investigative Site Sarasota Florida 34233
Novartis Investigative Site Tamarac Florida 33321
Novartis Investigator Site Couer D'Alene Idaho 83814
Novartis Investigator Site Champaign Illinois 61820
Novartis Investigator Site Downers Grove Illinois 60515
Novartis Investigative Site River Forest Illinois 60305
Novartis Investigator Site Skokie Illinois 60076
Novartis Investigator Site Springfield Illinois 62703
Novartis Investigative site Lexington Kentucky 40504
Novartis Investigator Site Covington Louisiana 70433
Novartis Investigator Site Metaire Louisiana 70002
Novartis Investigative Site Bangor Maine 04401
Novartis Investigative Site Columbia Maryland 21044
Novartis Investigative Site Clarkston Michigan 48346
Novartis Investigative Site Flint Michigan 48532
Novartis Investigative Site Livonia Michigan 48152
Novartis Investigative Site Edina Minnesota 55435
Novartis Investigative Site Minneapolis Minnesota 55402
Novartis Investigative Site Plymouth Minnesota 55441
Novartis Investigator Site Florissant Missouri 63033
Novartis Investigator Site Ozark Missouri 65721
Novartis Investigator Site St Louis Missouri 63117
Novartis Investigative Site Missoula Montana 59808
Novartis Investigator Site Bellevue Nebraska 68123
Novartis Investigator Site Lincoln Nebraska 68516
Novartis Investigator Site Omaha Nebraska 68134
Novartis Investigator Site Henderson Nevada 89014
Novartis Investigator Site Pahrump Nevada 89048
Novartis Investigative Site New Brunswick New Jersey 08902
Novartis Investigative Site Ocean City New Jersey 07712
Novartis Investigative Site Rochester New York 14618
Novartis Investigative Site Charlotte North Carolina 28209
Novartis Investigative Site Salisbury North Carolina 28144
Novartis Investigative Site Cincinnati Ohio 45231
Novartis Investigator Site Medford Oregon 97504
Novartis Investigative Site Beaver Pennsylvania 15009
Novartis Investigative Site Erie Pennsylvania 16506
Novartis Investigative Site Pittsburgh Pennsylvania 15221
Novartis Investigative Site Pittsburgh Pennsylvania 15243
Novartis Investigative Site Gaffney South Carolina 29340
Novartis Investigative site Greer South Carolina 29651
Novartis Investigative Site Seneca South Carolina 29678
Novartis Investigative Site Johnson City Tennessee 37601
Novartis Investigator Site Corsicana Texas 75110
Novartis Investigator Site Fort Worth Texas 76109
Novartis Investigator Site Salt Lake City Utah 84107
Novartis Investigator Site Abingdon Virginia 24210
Novartis Investigative Site Newport News Virginia 23606
Novartis Investigator Site Tacoma Washington 98405

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 NCT01072448, 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 Aug 18, 2011 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01072448 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →