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Terminated Phase 3 Interventional Results available

A Twelve Month Long Term Safety Study to Evaluate the Safety of Albuterol in a Dry Powder Inhaler With Both Repeated and as Needed Dosing

ClinicalTrials.gov ID: NCT01218009

Public ClinicalTrials.gov record NCT01218009. 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 29, 2026, 9:23 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 Multi-Center 52-Week Study to Assess the Safety of an Albuterol Dry-powder Inhaler in Subjects With Asthma

Study identification

NCT ID
NCT01218009
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Industry
Enrollment
331 participants

Conditions and interventions

Conditions

Interventions

  • Albuterol Spiromax Drug
  • Placebo Spiromax Drug

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
Sep 30, 2010
Primary completion
Nov 30, 2010
Completion
Nov 30, 2010
Last update posted
May 19, 2015

2010

United States locations

U.S. sites
30
U.S. states
19
U.S. cities
30
Facility City State ZIP Site status
Teva Clinical Study Site Scottsdale Arizona
Teva Clinical Study Site Los Angeles California
Teva Clinical Study Site San Diego California
Teva Clinical Study Site Centennial Colorado
Teva Clinical Study Site Denver Colorado
Teva Clinical Study Site Miami Florida
Teva Clinical Study Site Gainesville Georgia
Teva Clinical Study Site Louisville Kentucky
Teva Clinical Study Site Wheaton Maryland
Teva Clinical Study Site Minneapolis Minnesota
Teva Clinical Study Site Plymouth Minnesota
Teva Clinical Study Site St Louis Missouri
Teva Clinical Study Site Bellevue Nebraska
Teva Clinical Study Site Boys Town Nebraska
Teva Clinical Study Site Skillman New Jersey
Teva Clinical Study Site Rochester New York
Teva Clinical Study Site Rockville Centre New York
Teva Clinical Study Site High Point North Carolina
Teva Clinical Study Site Raleigh North Carolina
Teva Clinical Study Site Canton Ohio
Teva Clinical Study Site Cincinnati Ohio
Teva Clinical Study Site Sylvania Ohio
Teva Clinical Study Site Eugene Oregon
Teva Clinical Study Site Portland Oregon
Teva Clinical Study Site El Paso Texas
Teva Clinical Study Site New Braunfels Texas
Teva Clinical Study Site San Antonio Texas
Teva Clinical Study Site Burke Virginia
Teva Clinical Study Site Seattle Washington
Teva Clinical Study Site 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01218009, 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 May 19, 2015 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01218009 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →