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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 Oct 21, 2026, 7:05 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

Brief summary

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

The primary objective of this study is to evaluate the efficacy of Albuterol Spiromax® versus placebo in subjects with persistent asthma.

Study identification

NCT ID
NCT01747629
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
160 participants

Conditions and interventions

Conditions

Interventions

Drug

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
Dec 2012 (Type not available)
Primary completion
Oct 2013 (Actual)
Completion
Nov 2013 (Actual)
Last update posted
Jun 26, 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 26, 2015 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01747629 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →