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Completed Phase 3 Interventional Results available

Study of Fluticasone Propionate Multidose Dry Powder Inhaler Compared With Fluticasone Propionate/Salmeterol Multidose Dry Powder Inhaler

ClinicalTrials.gov ID: NCT02980133

Public ClinicalTrials.gov record NCT02980133. 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 17, 2026, 9:56 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, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Fluticasone Propionate Multidose Dry Powder Inhaler Compared With Fluticasone Propionate/Salmeterol Multidose Dry Powder Inhaler in Patients Aged 4 Through 11 Years With Persistent Asthma

Brief summary

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

This study is to evaluate the safety and efficacy of fluticasone propionate and fluticasone propionate salmeterol in pediatric participants with a documented history of persistent asthma.

Study identification

NCT ID
NCT02980133
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
841 participants

Conditions and interventions

Eligibility (public fields only)

Age range
4 Years to 11 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
Dec 28, 2016 (Actual)
Primary completion
Apr 7, 2019 (Actual)
Completion
Apr 13, 2019 (Actual)
Last update posted
Nov 9, 2021

2016 – 2019

United States locations

U.S. sites
77
U.S. states
25
U.S. cities
62
Facility City State ZIP Site status
Teva Investigational Site 13881 Birmingham Alabama 35209 —
Teva Investigational Site 13883 Little Rock Arkansas 72205 —
Teva Investigational Site 13906 Bakersfield California 93301 —
Teva Investigational Site 14615 Corona California 92883 —
Teva Investigational Site 13892 Downey California 90241 —
Teva Investigational Site 13875 Fountain Valley California 92708 —
Teva Investigational Site 13904 Huntington Beach California 92647 6818 —
Teva Investigational Site 13877 Huntington Beach California 92648 —
Teva Investigational Site 14668 Long Beach California 90806 —
Teva Investigational Site 13914 Napa California 94558 —
Teva Investigational Site 13918 Paramount California 90723 —
Teva Investigational Site 14618 Rolling Hills Estates California 90274 —
Teva Investigational Site 13912 Roseville California 95661 —
Teva Investigational Site 13847 Stockton California 95207 —
Teva Investigational Site 13848 Thousand Oaks California 91360 —
Teva Investigational Site 13856 Centennial Colorado 80112 —
Teva Investigational Site 13910 Colorado Springs Colorado 80907 —
Teva Investigational Site 13868 Longmont Colorado 80501 —
Teva Investigational Site 13913 Chiefland Florida 32626 —
Teva Investigational Site 14616 DeLand Florida 32720 —
Teva Investigational Site 13909 Homestead Florida 33030 —
Teva Investigational Site 13857 Loxahatchee Groves Florida 33470 —
Teva Investigational Site 13872 Miami Florida 33134 —
Teva Investigational Site 13907 Miami Florida 33134 —
Teva Investigational Site 13893 Miami Florida 33142 —
Teva Investigational Site 13886 Miami Florida 33155 —
Teva Investigational Site 13899 Miami Florida 33175 —
Teva Investigational Site 13864 Miami Florida 33176 —
Teva Investigational Site 13880 Miami Florida 33176 —
Teva Investigational Site 13870 Miami Lakes Florida 33014 —
Teva Investigational Site 14617 Miami Lakes Florida 33015 —
Teva Investigational Site 13916 Miami Springs Florida 33185 —
Teva Investigational Site 13911 Ocala Florida 34471 —
Teva Investigational Site 13876 Palmetto Bay Florida 33157 —
Teva Investigational Site 13844 Winter Park Florida 32789 —
Teva Investigational Site 13866 Gainesville Georgia 30501 —
Teva Investigational Site 13858 Savannah Georgia 31406 —
Teva Investigational Site 13896 Eagle Idaho 83616 —
Teva Investigational Site 13903 Idaho Falls Idaho 83402 —
Teva Investigational Site 13882 Springfield Illinois 62704 —
Teva Investigational Site 13887 Overland Park Kansas 66210 —
Teva Investigational Site 13851 Owensboro Kentucky 42301 —
Teva Investigational Site 13849 Rockville Maryland 20850 —
Teva Investigational Site 13865 Columbia Missouri 65203 —
Teva Investigational Site 13885 Columbia Missouri 65203 —
Teva Investigational Site 13891 Missoula Montana 59808 —
Teva Investigational Site 13897 Ocean City New Jersey 07712 —
Teva Investigational Site 13854 Verona New Jersey 07044 —
Teva Investigational Site 13908 Watertown New York 13601 —
Teva Investigational Site 13890 Charlotte North Carolina 28277 —
Teva Investigational Site 13863 Raleigh North Carolina 27607 —
Teva Investigational Site 13855 Canton Ohio 44718 —
Teva Investigational Site 13905 Milford Ohio 45150 —
Teva Investigational Site 13852 Oklahoma City Oklahoma 73112 —
Teva Investigational Site 13879 Oklahoma City Oklahoma 73112 —
Teva Investigational Site 13884 Oklahoma City Oklahoma 73120 —
Teva Investigational Site 13860 Tulsa Oklahoma 74136 —
Teva Investigational Site 13894 Tulsa Oklahoma 74136 —
Teva Investigational Site 13861 Medford Oregon 97504 —
Teva Investigational Site 13874 Pittsburgh Pennsylvania 15241 —
Teva Investigational Site 13895 Scottdale Pennsylvania 15683 —
Teva Investigational Site 13888 Providence Rhode Island 02909 —
Teva Investigational Site 13871 Charleston South Carolina 29407 —
Teva Investigational Site 13889 Charleston South Carolina 29414 —
Teva Investigational Site 13853 Spartanburg South Carolina 29303 —
Teva Investigational Site 14671 Summerville South Carolina 29483 —
Teva Investigational Site 13898 Baytown Texas 77521 —
Teva Investigational Site 14673 Boerne Texas 78006 —
Teva Investigational Site 13867 El Paso Texas 79903 —
Teva Investigational Site 13902 Killeen Texas 76542-0969 —
Teva Investigational Site 13846 Live Oak Texas 78233 —
Teva Investigational Site 13878 San Antonio Texas 78229 —
Teva Investigational Site 14672 San Antonio Texas 78229 —
Teva Investigational Site 13917 San Antonio Texas 78251 —
Teva Investigational Site 13845 Waco Texas 76712 —
Teva Investigational Site 13850 Richmond Virginia 23223 —
Teva Investigational Site 13915 Bellingham Washington 98225 —

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 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02980133, 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 Nov 9, 2021 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02980133 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →