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Completed Phase 3 Interventional Results available

Efficacy and Safety Study of FP MDPI Compared With FS MDPI in Adolescent and Adult Patients With Persistent Asthma

ClinicalTrials.gov ID: NCT02141854

Public ClinicalTrials.gov record NCT02141854. 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, 11:29 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, Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Fluticasone Propionate Multidose Dry Powder Inhaler Compared With Fluticasone/Salmeterol Multidose Dry Powder Inhaler in Adolescent and Adult Patients With Persistent Asthma Symptomatic Despite Inhaled Corticosteroid Therapy

Brief summary

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

The primary objective of this study was to evaluate the efficacy of fluticasone propionate (Fp) multidose dry powder inhaler (MDPI) and fluticasone propionate/salmeterol xinafoate (FS) MDPI when administered over 12 weeks in patients 12 years of age and older with persistent asthma.

Study identification

NCT ID
NCT02141854
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
882 participants

Conditions and interventions

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
Jun 2014 (Type not available)
Primary completion
Sep 2015 (Actual)
Completion
Sep 2015 (Actual)
Last update posted
Nov 9, 2021

2014 – 2015

United States locations

U.S. sites
85
U.S. states
33
U.S. cities
77
Facility City State ZIP Site status
Teva Investigational Site 12429 Birmingham Alabama — —
Teva Investigational Site 12599 Little Rock Alaska — —
Teva Investigational Site 12609 Phoenix Arizona — —
Teva Investigational Site 12445 Costa Mesa California — —
Teva Investigational Site 12454 Encinitas California — —
Teva Investigational Site 12456 Fresno California — —
Teva Investigational Site 12461 Fullerton California — —
Teva Investigational Site 12410 Huntington Beach California — —
Teva Investigational Site 12452 Huntington Beach California — —
Teva Investigational Site 12417 Long Beach California — —
Teva Investigational Site 13017 Mission Viejo California — —
Teva Investigational Site 12462 Rancho Mirage California — —
Teva Investigational Site 12411 Rolling Hills Estates California — —
Teva Investigational Site 13018 San Diego California — —
Teva Investigational Site 12413 San Jose California — —
Teva Investigational Site 12403 Stockton California — —
Teva Investigational Site 12444 Upland California — —
Teva Investigational Site 12999 Vista California — —
Teva Investigational Site 12405 Centennial Colorado — —
Teva Investigational Site 12419 Centennial Colorado — —
Teva Investigational Site 13000 Colorado Springs Colorado — —
Teva Investigational Site 12459 Waterbury Connecticut — —
Teva Investigational Site 13004 Largo Florida — —
Teva Investigational Site 12414 Miami Florida — —
Teva Investigational Site 12437 Miami Florida — —
Teva Investigational Site 12427 Orlando Florida — —
Teva Investigational Site 12423 Ormond Beach Florida — —
Teva Investigational Site 12604 Panama City Florida — —
Teva Investigational Site 13316 Tamarac Florida — —
Teva Investigational Site 12606 Winter Park Florida — —
Teva Investigational Site 12435 Savannah Georgia — —
Teva Investigational Site 13315 Eagle Idaho — —
Teva Investigational Site 12439 River Forest Illinois — —
Teva Investigational Site 12449 Shiloh Illinois — —
Teva Investigational Site 12457 South Bend Indiana — —
Teva Investigational Site 12446 Bangor Maine — —
Teva Investigational Site 12602 Columbia Maryland — —
Teva Investigational Site 12432 Fall River Massachusetts — —
Teva Investigational Site 12441 North Dartmouth Massachusetts — —
Teva Investigational Site 12466 North Dartmouth Massachusetts — —
Teva Investigational Site 13001 Royal Oak Michigan — —
Teva Investigational Site 12428 Ypsilanti Michigan — —
Teva Investigational Site 13020 Minneapolis Minnesota — —
Teva Investigational Site 12451 Columbia Missouri — —
Teva Investigational Site 12421 Rolla Missouri — —
Teva Investigational Site 12412 St Louis Missouri — —
Teva Investigational Site 12453 St Louis Missouri — —
Teva Investigational Site 12610 Missoula Montana — —
Teva Investigational Site 13021 Las Vegas Nevada — —
Teva Investigational Site 12409 Skillman New Jersey — —
Teva Investigational Site 12464 Brooklyn New York — —
Teva Investigational Site 12603 The Bronx New York — —
Teva Investigational Site 12430 Charlotte North Carolina — —
Teva Investigational Site 12407 Raleigh North Carolina — —
Teva Investigational Site 12415 Canton Ohio — —
Teva Investigational Site 12455 Cincinnati Ohio — —
Teva Investigational Site 12463 Cincinnati Ohio — —
Teva Investigational Site 12460 Middleburg Heights Ohio — —
Teva Investigational Site 12426 Edmond Oklahoma — —
Teva Investigational Site 13008 Oklahoma City Oklahoma — —
Teva Investigational Site 12406 Medford Oregon — —
Teva Investigational Site 12442 Portland Oregon — —
Teva Investigational Site 12563 Normal Square Pennsylvania — —
Teva Investigational Site 12443 Pittsburgh Pennsylvania — —
Teva Investigational Site 12438 Upland Pennsylvania — —
Teva Investigational Site 12408 Charleston South Carolina — —
Teva Investigational Site 12431 Greenville South Carolina — —
Teva Investigational Site 12465 Mt. Pleasant South Carolina — —
Teva Investigational Site 12467 Mt. Pleasant South Carolina — —
Teva Investigational Site 12420 Orangeburg South Carolina — —
Teva Investigational Site 12433 Rock Hill South Carolina — —
Teva Investigational Site 13003 Knoxville Tennessee — —
Teva Investigational Site 12425 Arlington Texas — —
Teva Investigational Site 12416 Dallas Texas — —
Teva Investigational Site 12418 Dallas Texas — —
Teva Investigational Site 12440 El Paso Texas — —
Teva Investigational Site 12447 Killeen Texas — —
Teva Investigational Site 13318 San Antonio Texas — —
Teva Investigational Site 13002 Sugar Land Texas — —
Teva Investigational Site 12424 Waco Texas — —
Teva Investigational Site 12422 South Burlington Vermont — —
Teva Investigational Site 12605 Richmond Virginia — —
Teva Investigational Site 12436 Spokane Washington — —
Teva Investigational Site 12564 Tacoma Washington — —
Teva Investigational Site 12448 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 69 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02141854, 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 NCT02141854 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →