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Completed Phase 2 Interventional

Confirmatory Dose Finding Study of 2 Dosages of CHF 4226 pMDI (Carmoterol) in Patients With COPD

ClinicalTrials.gov ID: NCT00640484

Public ClinicalTrials.gov record NCT00640484. 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 Nov 4, 2026, 12:26 PM EST

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Official title

Evaluation of the Effect of 2 Weeks Treatment With CHF 4226 pMDI 2µg and 4µg, Given Once Daily in the Morning, on 24-Hour FEV1 in Patients With COPD

Brief summary

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

The purpose of this study is to confirm the dose of CHF 4226 (carmoterol) that should be given once a day to patients with COPD in order for the effect to last for 24 hours.

Study identification

NCT ID
NCT00640484
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Chiesi Farmaceutici S.p.A.
Industry
Enrollment
57 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 75 Years
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
Apr 2008 (Type not available)
Primary completion
Oct 2008 (Actual)
Completion
Oct 2008 (Actual)
Last update posted
Aug 27, 2010

2008

United States locations

U.S. sites
15
U.S. states
13
U.S. cities
15
Facility City State ZIP Site status
Horizon Clinical Research Associates, PLLC Gilbert Arizona 85295 —
Pulmonary Associates, PA Phoenix Arizona 85006 —
UCLA David Geffen School of Medicine Los Angeles California 90095 —
University Clinical Research - DeLand, LLC DeLand Florida 32720 —
Pulmonary Medicine and Critical Care Austell Georgia 30106 —
Sneeze, Wheeze & Itch Associates, LLC Normal Illinois 61761 —
Commonwealth BioMedical Research Madisonville Kentucky 42431 —
North Carolina Clinical Research Raleigh North Carolina 27607 —
New Horizons Clinical Research Cincinnati Ohio 45242 —
Lynn Health Science Institute Oklahoma City Oklahoma 73112 —
Clinical Research Institute of Southern Oregon, PC Medford Oregon 97504 —
Asthma Allergy Associates Portland Oregon 97213 —
Spartanburg Medical Research Spartanburg South Carolina 29303 —
Reichman Associates Sugar Land Texas 77074 —
University of Utah Salt Lake City Utah 84108 —

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 NCT00640484, 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 27, 2010 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00640484 live on ClinicalTrials.gov.

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