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Completed Phase 3 Interventional Results available

Efficacy and Safety Study of QVA149 in COPD Patients

ClinicalTrials.gov ID: NCT02487446

Public ClinicalTrials.gov record NCT02487446. 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, 7:20 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 Multi-center, Randomized, Double-blind, Double-dummy, Active Controlled, 2-period Cross-over Study to Assess the Efficacy, Safety and Tolerability of Indacaterol Maleate/Glycopyrronium Bromide Compared to Umeclidinium Bromide/Vilanterol in COPD Patients With Moderate to Severe Airflow Limitation

Brief summary

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

The purpose of this study is to demonstrate that the efficacy of the combination product QVA149 is similar to the efficacy of the combination product umeclidinium/vilanterol on a pre-specified endpoint of FEV1 AUC0-24h while maintaining an acceptable safety profile.

Study identification

NCT ID
NCT02487446
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
357 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
Jul 28, 2015 (Actual)
Primary completion
Sep 12, 2016 (Actual)
Completion
Sep 12, 2016 (Actual)
Last update posted
Dec 26, 2017

2015 – 2016

United States locations

U.S. sites
58
U.S. states
21
U.S. cities
55
Facility City State ZIP Site status
Novartis Investigative Site Andalusia Alabama 36305 —
Novartis Investigative Site Anniston Alabama 36207-5710 —
Novartis Investigative Site Jasper Alabama 35501 —
Novartis Investigative Site Multiple Locations Alabama — —
Novartis Investigative Site Multiple Locations Arizona — —
Novartis Investigative Site Tempe Arizona 85283 —
Novartis Investigative Site Tucson Arizona 85723 —
Novartis Investigative Site Fayetteville Arkansas 72703 —
Novartis Investigative Site Huntington Beach California 92647 —
Novartis Investigative Site Rancho Mirage California 92270 —
Novartis Investigative Site Colorado Springs Colorado 80907 —
Novartis Investigative Site Altamonte Springs Florida 32701 —
Novartis Investigative Site DeLand Florida 32720 —
Novartis Investigative Site Fort Lauderdale Florida 33316-192 —
Novartis Investigative Site Kissimmee Florida 34741 —
Novartis Investigative Site Miami Florida 33172 —
Novartis Investigative Site Pensacola Florida 32503 —
Novartis Investigative Site Pensacola Florida 32504 —
Novartis Investigative Site Port Orange Florida 32127 —
Novartis Investigative Site Conyers Georgia 30094 —
Novartis Investigative Site Duluth Georgia 30096 —
Novartis Investigative Site Meridian Idaho 83642 —
Novartis Investigative Site New Orleans Louisiana 70119 —
Novartis Investigative Site Slidell Louisiana 70458 —
Novartis Investigative Site Sunset Louisiana 70584 —
Novartis Investigative Site Columbia Maryland 21044 —
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 Plymouth Minnesota 55441 —
Novartis Investigative Site Henderson Nevada 89014 —
Novartis Investigative Site New York New York 10016 —
Novartis Investigative Site Charlotte North Carolina 28207 —
Novartis Investigative Site Cornelius North Carolina 28031 —
Novartis Investigative Site Gastonia North Carolina 28054 —
Novartis Investigative Site Hickory North Carolina 28602 —
Novartis Investigative Site High Point North Carolina 27262 —
Novartis Investigative Site Huntersville North Carolina 28078 —
Novartis Investigative Site Winston-Salem North Carolina 27103 —
Novartis Investigative Site Cincinnati Ohio 45242 —
Novartis Investigative Site Columbus Ohio 43213 —
Novartis Investigative Site Columbus Ohio 43215 —
Novartis Investigative Site Dublin Ohio 43016 —
Novartis Investigative Site Marion Ohio 43302 —
Novartis Investigative Site Medford Oregon 97504 —
Novartis Investigative Site Portland Oregon 97213 —
Novartis Investigative Site Philadelphia Pennsylvania 19142 —
Novartis Investigative Site Tipton Pennsylvania 16684 —
Novartis Investigative Site Carrollton Texas 75010 —
Novartis Investigative Site Channelview Texas 77530 —
Novartis Investigative Site Fort Worth Texas 76109 —
Novartis Investigative Site Lampasas Texas 76550 —
Novartis Investigative Site McKinney Texas 75069 —
Novartis Investigative Site New Braunfels Texas 78130 —
Novartis Investigative Site Salt Lake City Utah 84102 —
Novartis Investigative Site Newport News Virginia 23606 —
Novartis Investigative 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 NCT02487446, 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 Dec 26, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02487446 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →