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Completed Phase 3 Interventional Results available

Efficacy of Inhaled Albuterol Spiromax® in Subjects With Persistent Asthma With Steady State Pharmacokinetics

ClinicalTrials.gov ID: NCT01747629

Public ClinicalTrials.gov record NCT01747629. 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 Apr 22, 2026, 11:55 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 Comparison of the Efficacy and Safety and Steady-State Pharmacokinetics of Albuterol Spiromax® Versus Placebo in Subjects 12 Years and Older With Persistent Asthma

Study identification

NCT ID
NCT01747629
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
160 participants

Conditions and interventions

Conditions

Interventions

  • Albuterol MDPI Drug
  • Placebo MDPI Drug

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2012
Primary completion
Sep 30, 2013
Completion
Oct 31, 2013
Last update posted
Jun 25, 2015

2012 – 2013

United States locations

U.S. sites
35
U.S. states
17
U.S. cities
33
Facility City State ZIP Site status
Teva Investigational Site 10225 Costa Mesa California
Teva Investigational Site 10250 Encinitas California
Teva Investigational Site 10230 Huntington Beach California
Teva Investigational Site 10255 Palmdale California
Teva Investigational Site 10231 Rancho Mirage California
Teva Investigational Site 10252 Riverside California
Teva Investigational Site 10242 Rolling Hills Estates California
Teva Investigational Site 10238 San Diego California
Teva Investigational Site 10243 San Jose California
Teva Investigational Site 10247 Miami Lakes Florida
Teva Investigational Site 10239 Tallahassee Florida
Teva Investigational Site 10234 Tampa Florida
Teva Investigational Site 10253 Bangor Maine
Teva Investigational Site 10257 Baltimore Maryland
Teva Investigational Site 10254 White Marsh Maryland
Teva Investigational Site 10235 Fall River Massachusetts
Teva Investigational Site 10236 North Dartmouth Massachusetts
Teva Investigational Site 10226 Minneapolis Minnesota
Teva Investigational Site 10233 Minneapolis Minnesota
Teva Investigational Site 10241 St Louis Missouri
Teva Investigational Site 10229 Bellevue Nebraska
Teva Investigational Site 10227 Rochester New York
Teva Investigational Site 10244 Charlotte North Carolina
Teva Investigational Site 10248 Cincinnati Ohio
Teva Investigational Site 10249 Oklahoma City Oklahoma
Teva Investigational Site 10232 Eugene Oregon
Teva Investigational Site 10259 Medford Oregon
Teva Investigational Site 10237 Portland Oregon
Teva Investigational Site 10240 Bethlehem Pennsylvania
Teva Investigational Site 10246 Pittsburgh Pennsylvania
Teva Investigational Site 10256 Pittsburgh Pennsylvania
Teva Investigational Site 10251 Rock Hill South Carolina
Teva Investigational Site 10228 Spartanburg South Carolina
Teva Investigational Site 10258 San Antonio Texas
Teva Investigational Site 10245 Seattle Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01747629, 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 25, 2015 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01747629 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →