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Completed Phase 3 Interventional Results available

Effect of Roflumilast on Exacerbation Rate in Patients With Chronic Obstructive Pulmonary Disease (COPD): The AURA Study (BY217/M2-124)

ClinicalTrials.gov ID: NCT00297102

Public ClinicalTrials.gov record NCT00297102. 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 28, 2026, 5:59 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

Effect of Roflumilast on Exacerbation Rate in Patients With COPD. The AURA Study

Brief summary

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

The aim of the study is to investigate the effect of roflumilast on exacerbation rate and pulmonary function in patients with chronic obstructive pulmonary disease (COPD). Roflumilast will be administered orally once daily in the morning at one dose level. The study duration will last up to 56 weeks. The study will provide further data on safety and tolerability of roflumilast. For additional information (for US patients only) see www.COPDSTUDY.net or dial 866-788-2673 (toll free).

Study identification

NCT ID
NCT00297102
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
1,523 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
Feb 2006 (Type not available)
Primary completion
Jul 2008 (Actual)
Completion
Sep 2008 (Actual)
Last update posted
Jan 16, 2017

2006 – 2008

United States locations

U.S. sites
47
U.S. states
26
U.S. cities
46
Facility City State ZIP Site status
Altana Pharma/Nycomed Investigational Site Fullerton California 92385 —
Altana Pharma/Nycomed Investigational Site Los Angeles California 90025 —
Altana Pharma/Nycomed Investigational Site Los Angeles California 90048 —
Altana Pharma/Nycomed Investigational Site Palmdale California 93551 —
Altana Pharma/Nycomed Investigational Site Rancho Mirage California 92270 —
Altana Pharma/Nycomed Investigational Site San Diego California 92120 —
Altana Pharma/Nycomed Investigational Site Bay Pines Florida 33708 —
Altana Pharma/Nycomed Investigational Site Miami Florida 33176 —
Altana Pharma/Nycomed Investigational Site Panama City Florida 32405 —
Altana Pharma/Nycomed Investigational Site Atlanta Georgia 30309 —
Altana Pharma/Nycomed Investigational Site Marietta Georgia 30060 —
Altana Pharma/Nycomed Investigational Site Hines Illinois 60141 —
Altana Pharma/Nycomed Investigational Site South Bend Indiana 46617 —
Altana Pharma/Nycomed Investigational Site Lebanon Kentucky 40291 —
Altana Pharma/Nycomed Investigational Site Metairie Louisiana 70006 —
Altana Pharma/Nycomed Investigational Site New Orleans Louisiana 70112 —
Altana Pharma/Nycomed Investigational Site Slidell Louisiana 70461 —
Altana Pharma/Nycomed Investigational Site Sunset Louisiana 70584 —
Altana Pharma/Nycomed Investigational Site Bangor Maine 04401 —
Altana Pharma/Nycomed Investigational Site Baltimore Maryland 21224 —
Altana Pharma/Nycomed Investigational Site North Dartmouth Massachusetts 02777 —
Altana Pharma/Nycomed Investigational Site Edina Minnesota 55435 —
Altana Pharma/Nycomed Investigational Site Minneapolis Minnesota 55407 —
Altana Pharma/Nycomed Investigational Site Chesterfield Missouri 63017 —
Altana Pharma/Nycomed Investigational Site St Louis Missouri 63117 —
Altana Pharma/Nycomed Investigational Site Billings Montana 59102 —
Altana Pharma/Nycomed Investigational Site Missoula Montana 59804 —
Altana Pharma/Nycomed Investigational Site Lincoln Nebraska 68510 —
Altana Pharma/Nycomed Investigational Site Omaha Nebraska 68114 —
Altana Pharma/Nycomed Investigational Site Reno Nevada 89502 —
Altana Pharma/Nycomed Investigational Site Cherry Hill New Jersey 08003 —
Altana Pharma/Nycomed Investigational Site Springfield New Jersey 07081 —
Altana Pharma/Nycomed Investigational Site New York New York 10029 —
Altana Pharma/Nycomed Investigational Site Winston-Salem North Carolina 27103 —
Altana Pharma/Nycomed Investigational Site Cincinnati Ohio 45241 —
Altana Pharma/Nycomed Investigational Site Columbus Ohio 43215 —
Altana Pharma/Nycomed Investigational Site Toledo Ohio 43614 —
Altana Pharma/Nycomed Investigational Site Youngstown Ohio 44501 —
Altana Pharma/Nycomed Investigational Site Lake Oswego Oregon 97035 —
Altana Pharma/Nycomed Investigational Site Philadelphia Pennsylvania 19140 —
Altana Pharma/Nycomed Investigational Site Cranston Rhode Island 02920 —
Altana Pharma/Nycomed Investigational Site East Providence Rhode Island 02914 —
Altana Pharma/Nycomed Investigational Site Austin Texas 78750 —
Altana Pharma/Nycomed Investigational Site Dallas Texas 75231 —
Altana Pharma/Nycomed Investigational Site Charlottesville, VA Virginia 22908 —
Altana Pharma/Nycomed Investigational Site Bellingham Washington 98225 —
Altana Pharma/Nycomed Investigational Site Marietta Wisconsin 53717 —

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 132 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00297102, 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 Jan 16, 2017 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00297102 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →