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Completed Phase 2 Interventional Results available

A Study of the Effectiveness and Safety of Different Doses of Fluticasone Propionate Taken From a Dry Powder Inhaler in Adolescents and Adults Who Have Asthma That is Not Controlled by Asthma Medications Not Containing Steroids

ClinicalTrials.gov ID: NCT01479621

Public ClinicalTrials.gov record NCT01479621. 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 2, 2026, 5:39 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 12-Week Dose-ranging Study to Evaluate the Efficacy and Safety of Fluticasone Propionate DPI Administered Twice Daily Compared With Placebo in Adolescent and Adult Subjects With Persistent Asthma Uncontrolled on Non-steroidal Therapy

Brief summary

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

This is a randomized, double-blind, placebo- and open-label active controlled, parallel-group, multicenter, dose ranging study in male or female subjects ages 12 years and older with persistent asthma who are uncontrolled on non-steroidal therapy. The primary objective of this study is to evaluate the dose response, efficacy and safety of 4 different doses of fluticasone propionate delivered as Fluticasone Propionate DPI (Dry Powder Inhaler) when administered twice daily.

Study identification

NCT ID
NCT01479621
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
909 participants

Conditions and interventions

Conditions

Eligibility (public fields only)

Age range
12 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
Dec 31, 2011
Primary completion
Jun 30, 2013
Completion
Jun 30, 2013
Last update posted
Jun 4, 2017

2012 – 2013

United States locations

U.S. sites
129
U.S. states
35
U.S. cities
107
Facility City State ZIP Site status
Teva Investigational Site 10165 Homewood Alabama
Teva Investigational Site 11142 Goodyear Arizona
Teva Investigational Site 10104 Scottsdale Arizona
Teva Investigational Site 11149 Little Rock Arkansas
Teva Investigational Site 10173 Bakersfield California
Teva Investigational Site 10163 Costa Mesa California
Teva Investigational Site 10156 Encinitas California
Teva Investigational Site 11101 Fountain Valley California
Teva Investigational Site 11111 Fresno California
Teva Investigational Site 10151 Granada Hills California
Teva Investigational Site 10157 Huntington Beach California
Teva Investigational Site 10176 Huntington Beach California
Teva Investigational Site 10147 Long Beach California
Teva Investigational Site 11110 Napa California
Teva Investigational Site 10136 Newport Beach California
Teva Investigational Site 11122 North Hollywood California
Teva Investigational Site 10140 Orange California
Teva Investigational Site 10197 Palmdale California
Teva Investigational Site 10185 Redwood City California
Teva Investigational Site 10143 Riverside California
Teva Investigational Site 11137 Roseville California
Teva Investigational Site 10130 San Diego California
Teva Investigational Site 10182 San Diego California
Teva Investigational Site 10179 San Jose California
Teva Investigational Site 10106 Stockton California
Teva Investigational Site 10129 Walnut Creek California
Teva Investigational Site 10145 Centennial Colorado
Teva Investigational Site 10172 Colorado Springs Colorado
Teva Investigational Site 10133 Denver Colorado
Teva Investigational Site 10154 Denver Colorado
Teva Investigational Site 11146 Denver Colorado
Teva Investigational Site 10128 Wheat Ridge Colorado
Teva Investigational Site 10196 Waterbury Connecticut
Teva Investigational Site 10191 Boynton Beach Florida
Teva Investigational Site 11127 Brandon Florida
Teva Investigational Site 11118 Clearwater Florida
Teva Investigational Site 11141 Hialeah Florida
Teva Investigational Site 11140 Kissimmee Florida
Teva Investigational Site 10137 Miami Florida
Teva Investigational Site 10153 Miami Florida
Teva Investigational Site 11120 Miami Florida
Teva Investigational Site 11128 Miami Florida
Teva Investigational Site 11132 Miami Florida
Teva Investigational Site 11145 Miami Florida
Teva Investigational Site 10171 Ocala Florida
Teva Investigational Site 10178 Sarasota Florida
Teva Investigational Site 11103 South Miami Florida
Teva Investigational Site 10161 Tallahassee Florida
Teva Investigational Site 10139 Tampa Florida
Teva Investigational Site 11114 Albany Georgia
Teva Investigational Site 10111 Columbus Georgia
Teva Investigational Site 11124 Columbus Georgia
Teva Investigational Site 10180 Gainesville Georgia
Teva Investigational Site 10168 Lawrenceville Georgia
Teva Investigational Site 11109 Idaho Falls Idaho
Teva Investigational Site 10116 Meridian Idaho
Teva Investigational Site 10127 South Bend Indiana
Teva Investigational Site 10184 Iowa City Iowa
Teva Investigational Site 10113 Metairie Louisiana
Teva Investigational Site 10164 Bangor Maine
Teva Investigational Site 10158 Bethesda Maryland
Teva Investigational Site 10110 Largo Maryland
Teva Investigational Site 10177 Wheaton Maryland
Teva Investigational Site 10138 North Dartmouth Massachusetts
Teva Investigational Site 10146 North Dartmouth Massachusetts
Teva Investigational Site 10131 Minneapolis Minnesota
Teva Investigational Site 10175 St Louis Missouri
Teva Investigational Site 10189 St Louis Missouri
Teva Investigational Site 11147 St Louis Missouri
Teva Investigational Site 10118 Bellevue Nebraska
Teva Investigational Site 10150 Omaha Nebraska
Teva Investigational Site 11144 Omaha Nebraska
Teva Investigational Site 11136 Henderson Nevada
Teva Investigational Site 10114 Brick New Jersey
Teva Investigational Site 10193 Cherry Hill New Jersey
Teva Investigational Site 10101 Hillsborough New Jersey
Teva Investigational Site 10155 Skillman New Jersey
Teva Investigational Site 10188 West Orange New Jersey
Teva Investigational Site 11113 Albuquerque New Mexico
Teva Investigational Site 10187 Brooklyn New York
Teva Investigational Site 10120 New York New York
Teva Investigational Site 10190 Newburgh New York
Teva Investigational Site 10167 North Syracuse New York
Teva Investigational Site 10112 Rochester New York
Teva Investigational Site 10105 High Point North Carolina
Teva Investigational Site 10122 Raleigh North Carolina
Teva Investigational Site 10194 Canton Ohio
Teva Investigational Site 10107 Cincinnati Ohio
Teva Investigational Site 10123 Cincinnati Ohio
Teva Investigational Site 10144 Columbus Ohio
Teva Investigational Site 11135 Dayton Ohio
Teva Investigational Site 11115 Middleburg Heights Ohio
Teva Investigational Site 10160 Oklahoma City Oklahoma
Teva Investigational Site 10174 Oklahoma City Oklahoma
Teva Investigational Site 10198 Oklahoma City Oklahoma
Teva Investigational Site 11108 Ashland Oregon
Teva Investigational Site 10132 Eugene Oregon
Teva Investigational Site 10135 Medford Oregon
Teva Investigational Site 10142 Portland Oregon
Teva Investigational Site 11104 Normal Square Pennsylvania
Teva Investigational Site 10183 Philadelphia Pennsylvania
Teva Investigational Site 10166 Pittsburgh Pennsylvania
Teva Investigational Site 10121 Upland Pennsylvania
Teva Investigational Site 11119 East Providence Rhode Island
Teva Investigational Site 10181 Lincoln Rhode Island
Teva Investigational Site 10162 Providence Rhode Island
Teva Investigational Site 10126 Charleston South Carolina
Teva Investigational Site 10149 Charleston South Carolina
Teva Investigational Site 10199 Orangeburg South Carolina
Teva Investigational Site 11131 Spartanburg South Carolina
Teva Investigational Site 10119 Boerne Texas
Teva Investigational Site 10141 Dallas Texas
Teva Investigational Site 10192 Dallas Texas
Teva Investigational Site 10148 El Paso Texas
Teva Investigational Site 10115 San Antonio Texas
Teva Investigational Site 11133 San Antonio Texas
Teva Investigational Site 11134 San Antonio Texas
Teva Investigational Site 10103 Waco Texas
Teva Investigational Site 11143 Layton Utah
Teva Investigational Site 10195 Provo Utah
Teva Investigational Site 10134 South Burlington Vermont
Teva Investigational Site 10159 Burke Virginia
Teva Investigational Site 10102 Fairfax Virginia
Teva Investigational Site 11105 Manassas Virginia
Teva Investigational Site 10108 Richmond Virginia
Teva Investigational Site 10124 Spokane Washington
Teva Investigational Site 11117 Tacoma Washington
Teva Investigational Site 11125 Tacoma Washington
Teva Investigational Site 10170 Greenfield Wisconsin

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 60 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01479621, 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 Jun 4, 2017 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01479621 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →