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Completed Phase 2 Interventional Results available

Dose-range Finding Efficacy and Safety Study for QBW251 in COPD Patients

ClinicalTrials.gov ID: NCT04072887

Public ClinicalTrials.gov record NCT04072887. 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 1, 2026, 11:13 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 24-week Multi-center, Double-blind, Placebo Controlled Dose-range Finding Study to Investigate the Efficacy and Safety of Oral QBW251 in COPD Patients on Triple Inhaled Therapy (LABA / LAMA / ICS)

Brief summary

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

This clinical study was designed to support the dose selection for future studies by evaluating efficacy and safety of different QBW251 doses in Chronic obstructive pulmonary disease (COPD) patients with chronic bronchitis and a history of exacerbations, compared to placebo, when added to a triple inhaled therapy of LABA, LAMA and ICS.

Study identification

NCT ID
NCT04072887
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
974 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
Sep 11, 2019
Primary completion
Oct 7, 2021
Completion
Jan 31, 2022
Last update posted
Apr 27, 2023

2019 – 2022

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
25
Facility City State ZIP Site status
Novartis Investigative Site Andalusia Alabama 36420
Novartis Investigative Site Los Angeles California 90025
Novartis Investigative Site Westminster California 92683
Novartis Investigative Site Ormond Beach Florida 32174
Novartis Investigative Site Sarasota Florida 34233
Novartis Investigative Site Winter Park Florida 32789
Novartis Investigative Site Florence Kentucky 41042
Novartis Investigative Site Crowley Louisiana 70526
Novartis Investigative Site New Orleans Louisiana 70115
Novartis Investigative Site Zachary Louisiana 70791
Novartis Investigative Site Livonia Michigan 48152
Novartis Investigative Site Edina Minnesota 55435
Novartis Investigative Site Minneapolis Minnesota 55407
Novartis Investigative Site Saint Charles Missouri 63301
Novartis Investigative Site St Louis Missouri 63141
Novartis Investigative Site Omaha Nebraska 68134
Novartis Investigative Site Charlotte North Carolina 28207
Novartis Investigative Site Gastonia North Carolina 28054
Novartis Investigative Site Shelby North Carolina 28150
Novartis Investigative Site Columbus Ohio 43215
Novartis Investigative Site Medford Oregon 97504
Novartis Investigative Site El Paso Texas 79903
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site McKinney Texas 75069
Novartis Investigative Site Midlothian Virginia 23114

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 123 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04072887, 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 Apr 27, 2023 · Synced Sep 1, 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 protocol, eligibility criteria, and contact information for NCT04072887 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →