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Completed Phase 3 Interventional Results available

Study of Fluticasone Propionate MDPI Compared With Fluticasone/Salmeterol MDPI in Adolescent and Adult Patients With Persistent Asthma

ClinicalTrials.gov ID: NCT02139644

Public ClinicalTrials.gov record NCT02139644. 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, 9:13 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 Low-dose or or Mid-dose 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 multidose dry powder inhaler (Fp MDPI) and fluticasone propionate/salmeterol xinafoate multidose dry powder inhaler (FS MDPI) when administered over 12 weeks in patients 12 years of age and older with persistent asthma. Study drug and placebo was supplied in Teva multidose dry powder inhaler (MDPI) devices and provided for participants to use at home. Participants performed spirometry at every visit. Each participant was given a diary at each visit for use until the next visit. Rescue medication (albuterol/salbutamol) was dispensed at each visit, if needed, as determined by the investigational center personnel.

Study identification

NCT ID
NCT02139644
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
787 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 12, 2021

2014 – 2015

United States locations

U.S. sites
76
U.S. states
27
U.S. cities
67
Facility City State ZIP Site status
Teva Investigational Site 12397 Birmingham Alabama — —
Teva Investigational Site 12375 Glendale Arizona — —
Teva Investigational Site 12395 Cypress California — —
Teva Investigational Site 12476 Encinitas California — —
Teva Investigational Site 12586 Fountain Valley California — —
Teva Investigational Site 12591 Fresno California — —
Teva Investigational Site 12372 Huntington Beach California — —
Teva Investigational Site 12365 Los Angeles California — —
Teva Investigational Site 12381 Los Angeles California — —
Teva Investigational Site 12401 Los Angeles California — —
Teva Investigational Site 12394 Mission Viejo California — —
Teva Investigational Site 12490 Rancho Mirage California — —
Teva Investigational Site 12393 Riverside California — —
Teva Investigational Site 12366 Rolling Hills Estates California — —
Teva Investigational Site 12383 San Diego California — —
Teva Investigational Site 12370 San Jose California — —
Teva Investigational Site 12371 Stockton California — —
Teva Investigational Site 12579 Upland California — —
Teva Investigational Site 12379 Centennial Colorado — —
Teva Investigational Site 12386 Centennial Colorado — —
Teva Investigational Site 12596 Colorado Springs Colorado — —
Teva Investigational Site 12584 Longmont Colorado — —
Teva Investigational Site 12484 Waterbury Connecticut — —
Teva Investigational Site 12590 Waterbury Connecticut — —
Teva Investigational Site 12493 Clearwater Florida — —
Teva Investigational Site 12992 Largo Florida — —
Teva Investigational Site 12376 Miami Florida — —
Teva Investigational Site 12390 Miami Florida — —
Teva Investigational Site 12583 Orlando Florida — —
Teva Investigational Site 12481 Tallahassee Florida — —
Teva Investigational Site 12491 Winter Park Florida — —
Teva Investigational Site 12997 Decatur Georgia — —
Teva Investigational Site 12392 Savannah Georgia — —
Teva Investigational Site 12592 Shiloh Illinois — —
Teva Investigational Site 12483 Lenexa Kansas — —
Teva Investigational Site 12399 Baltimore Maryland — —
Teva Investigational Site 12391 Bethesda Maryland — —
Teva Investigational Site 12589 Columbia Maryland — —
Teva Investigational Site 12369 Rockville Maryland — —
Teva Investigational Site 12396 Fall River Massachusetts — —
Teva Investigational Site 12384 North Dartmouth Massachusetts — —
Teva Investigational Site 12585 North Dartmouth Massachusetts — —
Teva Investigational Site 12588 Ypsilanti Michigan — —
Teva Investigational Site 12494 St Louis Missouri — —
Teva Investigational Site 12595 St Louis Missouri — —
Teva Investigational Site 12594 Missoula Montana — —
Teva Investigational Site 12385 Ocean City New Jersey — —
Teva Investigational Site 12380 Skillman New Jersey — —
Teva Investigational Site 12587 Brooklyn New York — —
Teva Investigational Site 12485 Rockville Centre New York — —
Teva Investigational Site 12475 Huntersville North Carolina — —
Teva Investigational Site 12364 Raleigh North Carolina — —
Teva Investigational Site 12374 Canton Ohio — —
Teva Investigational Site 12480 Cincinnati Ohio — —
Teva Investigational Site 12492 Cincinnati Ohio — —
Teva Investigational Site 12487 Middleburg Heights Ohio — —
Teva Investigational Site 12488 Sylvania Ohio — —
Teva Investigational Site 12377 Edmond Oklahoma — —
Teva Investigational Site 12368 Medford Oregon — —
Teva Investigational Site 12382 Portland Oregon — —
Teva Investigational Site 12400 Pittsburgh Pennsylvania — —
Teva Investigational Site 12473 Upland Pennsylvania — —
Teva Investigational Site 12389 Greenville South Carolina — —
Teva Investigational Site 12580 Mt. Pleasant South Carolina — —
Teva Investigational Site 12398 Orangeburg South Carolina — —
Teva Investigational Site 12991 Knoxville Tennessee — —
Teva Investigational Site 12990 Cypress Texas — —
Teva Investigational Site 12373 Dallas Texas — —
Teva Investigational Site 12402 El Paso Texas — —
Teva Investigational Site 12582 New Braunfels Texas — —
Teva Investigational Site 12363 San Antonio Texas — —
Teva Investigational Site 12482 San Antonio Texas — —
Teva Investigational Site 12477 Waco Texas — —
Teva Investigational Site 12478 Murray Utah — —
Teva Investigational Site 12388 South Burlington Vermont — —
Teva Investigational Site 12378 Milwaukee 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 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02139644, 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 12, 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 NCT02139644 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →