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Completed Phase 3 Interventional Results available

Efficacy and Safety of Indacaterol Plus Tiotropium Versus Tiotropium Alone in Patients With Chronic Obstructive Pulmonary Disease

ClinicalTrials.gov ID: NCT00846586

Public ClinicalTrials.gov record NCT00846586. 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, 9:15 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 Randomized, Double-blind, Controlled, Parallel-group, 12-week Study to Compare the Efficacy and Safety of the Combination of Indacaterol 150 µg Once Daily With Open Label Tiotropium 18 µg Once Daily Versus Open Label Tiotropium 18 µg Once Daily in Patients With Moderate-to-severe Chronic Obstructive Pulmonary Disease

Brief summary

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

This study assessed the efficacy and safety of indacaterol (150 µg once daily \[od\]) when combined with tiotropium (18 µg od) versus tiotropium (18 µg od) treatment alone in patients with chronic obstructive pulmonary disease (COPD)

Study identification

NCT ID
NCT00846586
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,134 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
Mar 2009 (Type not available)
Primary completion
Mar 2010 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
Aug 18, 2011

2009 – 2010

United States locations

U.S. sites
61
U.S. states
30
U.S. cities
56
Facility City State ZIP Site status
Novartis Investigator Site Birmingham Alabama 32509 —
Novartis Investigator Site Mobile Alabama 36608 —
Novartis Investigative Site Scottsdale Arizona 85258 —
Novartis Investigative Site Tucson Arizona 85712 —
Novartis Investigative Site Tucson Arizona 85723 —
Novartis Investigator Site Pine Bluff Arkansas 71603 —
Novartis Investigator Site Fountain Valley California 92708 —
Novartis Investigator Site Long Beach California 90822 —
Novartis Investigative Site Los Angeles California 90095 —
Novartis Investigator Site National City California 91950 —
Novartis Investigator Site Palmdale California 93551 —
Novartis Investigative Site Stockton California 95207 —
Novartis Investigator Site Temecula California 92591 —
Novartis Investigative Site Hartford Connecticut 06105-1208 —
Novartis Investigative Site Clearwater Florida 33756 —
Novartis Investigator Site Fort Walton Beach Florida 32547 —
Novartis Investigative Site Miami Florida 33136 —
Novartis Investigative Site Miami Florida 331577 —
Novartis Investigative Site Naranja Florida 33032 —
Novartis Investigator Site Pensacola Florida 32514 —
Novartis Investigator Site Sarasota Florida 34233 —
Novartis Investigative Site Atlanta Georgia 30342 —
Novartis Investigator Site Conyers Georgia 30094 —
Novartis Investigative Site Normal Illinois 61761 —
Novartis Investigative Site Iowa City Iowa 52240 —
Novartis Investigative Site Kansas City Kansas 66160 —
Novartis Investigative Site Lenexa Kansas 66215 —
Novartis Investigative Site Topeka Kansas 66606 —
Novartis Investigator Site Lafayette Louisiana 70503 —
Novartis Investigator Site Metaire Louisiana 70002 —
Novartis Investigator Site New Orleans Louisiana 70119 —
Novartis Investigator Site Slidell Louisiana 70458 —
Novartis Investigator Site Columbia Maryland 21044 —
Novartis Investigator Site Brockton Massachusetts 02301 —
Novartis Investigator Site Clarkston Michigan 48346 —
Novartis Investigator Site Detroit Michigan 48202 —
Novartis Investigative Site Saint Charles Missouri 63301 —
Novartis Investigator Site Missoula Montana 59808 —
Novartis Investigator Site Boys Town Nebraska 68010 —
Novartis Investigative Site Omaha Nebraska 68114 —
Novartis Investigative site Omaha Nebraska 68134 —
Novartis Investigative Site Las Vegas Nevada 89119 —
Novartis Investigator Site Lebanon New Hampshire 03756 —
Novartis Investigator Site Asbury Park New Jersey 07712 —
Novartis Investigative Site Rochester New York 14618 —
Novartis Investigator Site Mooresville North Carolina 28117 —
Novartis Investigative Site Winston-Salem North Carolina 27103 —
Novartis Investigator Site Tulsa Oklahoma 74135-2920 —
Novartis Investigative Site Medford Oregon 97504 —
Novartis Investigator Site Bethlehem Pennsylvania 18020 —
Novartis Investigative Site Cumberland Rhode Island 02864 —
Novartis Investigator Site Greenville South Carolina 29615 —
Novartis Investigative Site Spartanburg South Carolina 29303 —
Novartis Investigator Site Knoxville Tennessee 37919 —
Novartis Investigator Site El Paso Texas 79903 —
Novartis Investigative Site Houston Texas 77024 —
Novartis Investigative Site Houston Texas 77079 —
Novartis Investigative Center New Braunfels Texas 78130-6113 —
Novartis Investigator Site Newport News Virginia 23606 —
Novartis Investigative Site Richmond Virginia 23225 —
Novartis Investigator Site Richmond Virginia 23249 —

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 76 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00846586, 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 Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00846586 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →