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Completed Phase 3 Interventional Results available

A Chronic-Dose Safety and Efficacy Study of Albuterol Multi-Dose Dry Powder Inhaler in Pediatric Asthmatics

ClinicalTrials.gov ID: NCT02126839

Public ClinicalTrials.gov record NCT02126839. 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 19, 2026, 11:35 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 Three-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Chronic-Dose Safety and Efficacy Study of Albuterol Multi-Dose Dry Powder Inhaler (MDPI) Relative to Placebo in Pediatric Asthmatics

Brief summary

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

The study is to evaluate the chronic-dose efficacy and the safety of Albuterol MDPI compared to placebo in pediatric participants with asthma.

Study identification

NCT ID
NCT02126839
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
186 participants

Conditions and interventions

Conditions

Interventions

Drug

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

2014 – 2015

United States locations

U.S. sites
51
U.S. states
21
U.S. cities
48
Facility City State ZIP Site status
Teva Investigational Site 12496 Birmingham Alabama — —
Teva Investigational Site 12500 Mobile Alabama — —
Teva Investigational Site 12481 Little Rock Alaska — —
Teva Investigational Site 12515 Anaheim California — —
Teva Investigational Site 12505 Costa Mesa California — —
Teva Investigational Site 12476 Huntington Beach California — —
Teva Investigational Site 12519 Los Angeles California — —
Teva Investigational Site 12484 Mission Viejo California — —
Teva Investigational Site 12510 Riverside California — —
Teva Investigational Site 12483 Rolling Hills Estates California — —
Teva Investigational Site 12511 Sacramento California — —
Teva Investigational Site 12485 Stockton California — —
Teva Investigational Site 12512 Centennial Colorado — —
Teva Investigational Site 12522 Gainesville Florida — —
Teva Investigational Site 12535 Hollywood Florida — —
Teva Investigational Site 12526 Miami Florida — —
Teva Investigational Site 12516 Orlando Florida — —
Teva Investigational Site 12517 Tamarac Florida — —
Teva Investigational Site 12527 Vero Beach Florida — —
Teva Investigational Site 12513 Winter Park Florida — —
Teva Investigational Site 12486 Gainesville Georgia — —
Teva Investigational Site 12497 Lawrenceville Georgia — —
Teva Investigational Site 12480 Savannah Georgia — —
Teva Investigational Site 12508 Shiloh Illinois — —
Teva Investigational Site 12518 Iowa City Iowa — —
Teva Investigational Site 12523 Covington Louisiana — —
Teva Investigational Site 12495 Warrensburg Missouri — —
Teva Investigational Site 12509 Northfield New Jersey — —
Teva Investigational Site 12524 Brooklyn New York — —
Teva Investigational Site 12473 Raleigh North Carolina — —
Teva Investigational Site 12477 Cincinnati Ohio — —
Teva Investigational Site 12525 Cleveland Ohio — —
Teva Investigational Site 12502 Middleburg Heights Ohio — —
Teva Investigational Site 12478 Oklahoma City Oklahoma — —
Teva Investigational Site 12487 Oklahoma City Oklahoma — —
Teva Investigational Site 12506 Oklahoma City Oklahoma — —
Teva Investigational Site 12492 Tulsa Oklahoma — —
Teva Investigational Site 12507 Gresham Oregon — —
Teva Investigational Site 12501 Normal Square Pennsylvania — —
Teva Investigational Site 12493 Pittsburgh Pennsylvania — —
Teva Investigational Site 12488 Upland Pennsylvania — —
Teva Investigational Site 12514 Greenville South Carolina — —
Teva Investigational Site 12474 Orangeburg South Carolina — —
Teva Investigational Site 12479 Spartanburg South Carolina — —
Teva Investigational Site 12489 Boerne Texas — —
Teva Investigational Site 12475 Waco Texas — —
Teva Investigational Site 12491 Burke Virginia — —
Teva Investigational Site 12504 Charlottesville Virginia — —
Teva Investigational Site 12482 Richmond Virginia — —
Teva Investigational Site 12498 Richmond Virginia — —
Teva Investigational Site 12490 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02126839, 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 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02126839 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →