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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 Oct 17, 2026, 4:45 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 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
Jan 2010 (Type not available)
Primary completion
Jul 2010 (Actual)
Completion
Jul 2010 (Actual)
Last update posted
Aug 19, 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 19, 2011 · Synced Oct 17, 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 public registry record, listed eligibility criteria, and available contact information for NCT01072448 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →