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Completed Phase 3 Interventional Results available

Safety, Tolerability and Efficacy of Indacaterol in Patients With Moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT00677807

Public ClinicalTrials.gov record NCT00677807. 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 21, 2026, 7:22 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 Extension to a 26-week Treatment, Multicenter, Randomized, Double-blind, Placebo-controlled, Adaptive, Seamless, Parallel-group Study to Assess Safety, Tolerability and Efficacy of Two Doses of Indacaterol (150 and 300 µg o.d.) in Patients With Chronic Obstructive Pulmonary Disease

Brief summary

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

This study evaluated the 1 year safety, tolerability and efficacy of indacaterol against placebo in the treatment of Chronic Obstructive Pulmonary Disease (COPD) patients

Study identification

NCT ID
NCT00677807
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis
Industry
Enrollment
415 participants

Conditions and interventions

Conditions

Interventions

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
May 2008 (Type not available)
Primary completion
Mar 2009 (Actual)
Completion
Mar 2009 (Actual)
Last update posted
Aug 22, 2011

2008 – 2009

United States locations

U.S. sites
93
U.S. states
35
U.S. cities
86
Facility City State ZIP Site status
Novartis Investigative Site Homewood Alabama 35209-6870 —
Novartis Investigative Site Jasper Alabama 35501 —
Novartis Investigative Site Phoenix Arizona 85013 —
Novartis Investigative Site Tucson Arizona 85712 —
Novartis Investigative Site Pine Bluff Arkansas 71603 —
Novartis Investigative Site Encinitas California 92024-1332 —
Novartis Investigative SIte Fullerton California 92835 —
Novartis Investigative Site Orange California 92869 —
Novartis Investigative Site Riverside California 92506 —
Novartis Investigative Site Spring Valley California 91978 —
Novartis Investigative site Fort Collins Colorado 80528 —
Novartis Investigative site Golden Colorado 80401 —
Novartis Investigative Site Wheat Ridge Colorado 80033 —
Novartis Investigative Site Clearwater Florida 33765 —
Novartis Investigative Site Largo Florida 33770 —
Novartis Investigative Site Pensacola Florida 32504 —
Novartis Investigative Site Rockledge Florida 32955 —
Novartis Investigative Site South Miami Florida 33143 —
Novartis Investigative Site Tamarac Florida 33321 —
Novartis Investigative Site Tampa Florida 33603 —
Novartis Investigative Site Atlanta Georgia 30342 —
Novartis Investigative Site Marietta Georgia 30060 —
Novartis Investigative Site Normal Illinois 61761 —
Novartis Investigative Site O'Fallon Illinois 62269 —
Novartis Investigative Site River Forest Illinois 60305 —
Novartis Investigative Site Indianapolis Indiana 46256 —
Novartis Investigative Site Iowa City Iowa 52240 —
Novartis Investigative Site Iowa City Iowa 52242 —
Novartis Investigative Site Topeka Kansas 66606 —
Novartis Investigative Site Crescent Springs Kentucky 41017 —
Novartis Investigative Site Lexington Kentucky 40504 —
Novartis Investigative Site Lexington Kentucky 40536 —
Novartis Investigative Site Lafayette Louisiana 70503 —
Novartis Investigative Site Metaire Louisiana 70002 —
Novartis Investigative site New Orleans Louisiana 70112 —
Novartis Investigative Site Biddeford Maine 04005 —
Novartis Investgative Site Clarkston Michigan 48346 —
Novartis Investigative Site Flint Michigan 48532 —
Novartis Investigative Site Livonia Michigan 48152 —
Novartis Investigative site Troy Michigan 48085 —
Novartis Investigative Site Minneapolis Minnesota 55402 —
Novartis Investigative Site Minneapolis Minnesota 55407 —
Novartis Investigative Site Rochester Minnesota 55905 —
Novartis Investigative Site Chesterfield Missouri 63017 —
Novartis Investigative Site Columbia Missouri 65212 —
Novartis Investigative Site Kansas City Missouri 64108-2677 —
Novartis Investigative Site St Louis Missouri 63141 —
Novartis Investigative Site Billings Montana 59102 —
Novartis Investigative Site Kalispell Montana 59901 —
Novartis Investigative Site Lincoln Nebraska 68510 —
Novartis Investigative Site Omaha Nebraska 68130 —
Novartis Investigative Site Omaha Nebraska 68134 —
Novartis Investigative Site Omaha Nebraska 68198-5885 —
Novartis Investigative Site Papillion Nebraska 68046 —
Novartis Investigative site Henderson Nevada 89014 —
Novartis Investigative site Summit New Jersey 07901 —
Novartis Investigative Site Elmira New York 14905 —
Novartis Investigative site New York New York 10016 —
Novartis Investigative Site Rochester New York 14618-2638 —
Novartis Investigative Site Charlotte North Carolina 28207 —
Novartis Investigative Site Shelby North Carolina 28150 —
Novartis Investigative Site Winston-Salem North Carolina 27103 —
Novartis Investigative Site Fargo North Dakota 58122 —
Novartis Investigative Site Cincinnati Ohio 45245 —
Novartis Investigative Site Cleveland Ohio 44109-1998 —
Novartis Investigative Site Columbus Ohio 43213 —
Novartis Investigative Site Columbus Ohio 43215 —
Novartis Investigative Site Marion Ohio 43302 —
Novartis Investigative Site Sylvania Ohio 43650 —
Novartis Investigative Site Thornville Ohio 43076 —
Novartis Investigative Site Zanesville Ohio 43701 —
Novartis Investigative Site Oklahoma City Oklahoma 73104 —
Novartis Investigative Site Tulsa Oklahoma 74135-2920 —
Novartis Investigative Site Eugene Oregon 97404-3233 —
Novartis Investigative Site Medford Oregon 97504-8741 —
Novartis Investigative Site Erie Pennsylvania 16506 —
Novartis Investigative Site Pittsburgh Pennsylvania 15221 —
Novartis Investigative Site Pittsburgh Pennsylvania 15243 —
Novartis Investigative site Cranston Rhode Island 02920 —
Novartis Investigative Site Cumberland Rhode Island 02864 —
Novartis Investigative Site Greenville South Carolina 29615 —
Novartis Investigative Site Johnson City Tennessee 37601 —
Novartis Investigative Site Corsicana Texas 75110 —
Novartis Investigative Site Dallas Texas 75231 —
Novartis Investigative site El Paso Texas 79902 —
Novartis Investigative Site Fort Worth Texas 76104 —
Novartis Investigative Site San Antonio Texas 78229 —
Novartis Investigative Site Abingdon Virginia 24210 —
Novartis Investigative site Lynchburg Virginia 24501 —
Novartis Investigative Site Richmond Virginia 23249 —
Novartis Investigative Site Bellingham Washington 98225 —
Novartis Investigative site Spokane Washington 99216 —
Novartis Investigative Site Milwaukee Wisconsin 53209-0996 —

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 97 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00677807, 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 22, 2011 · Synced Oct 21, 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 NCT00677807 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →