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Completed Phase 2 Interventional

A Trial to Assess the Pharmacodynamic Response in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT01168310

Public ClinicalTrials.gov record NCT01168310. 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 5, 2026, 12:37 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 12-week Randomized, Multiple-Dose, Double-Blind, Placebo-Controlled, Parallel-Group Trial to Assess the Pharmacodynamic Response of Fluticasone Propionate in Fixed-Dose Combination With Formoterol Fumarate in Subjects With COPD

Brief summary

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

This is a randomized, double-blind, multi-dose, parallel group trial which will assess the pharmacodynamic response of fluticasone propionate and formoterol fumarate in subjects with COPD.

Study identification

NCT ID
NCT01168310
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dey
Industry
Enrollment
468 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Days 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 31, 2010
Primary completion
Jul 31, 2010
Completion
Sep 30, 2011
Last update posted
May 26, 2013

2010 – 2011

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
Investigative Site Phoenix Arizona
Investigative Site Fullerton California
Investigative Site San Diego California
Investigative Site Clearwater Florida
Investigative Site DeLand Florida
Investigative Site Tamarac Florida
Investigative Site Lawrenceville Georgia
Investigative Site Coeur d'Alene Idaho
Investigative Site Madisonville Kentucky
Investigative Site Sunset Louisiana
Investigative Site St Louis Missouri
Investigative Site Charlotte North Carolina
Investigative Site Raleigh North Carolina
Investigative site Sylvania Ohio
Investigative Site Medford Oregon
Investigative Site Easley South Carolina
Investigative Site Gaffney South Carolina
Investigative Site Greenville South Carolina
Investigative Site Greer South Carolina
Investigative Site Spartanburg South Carolina
Invesigative Site Union South Carolina
Investigative Site San Antonio Texas
Investigative Site Spokane Washington

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 NCT01168310, 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 May 26, 2013 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01168310 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →