Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
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 Oct 24, 2026, 10:42 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

Brief summary

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

This is a one-year study to look at the safety of a dry powder inhaler with albuterol. After a one-week run in, for the first 3 months subjects will use an inhaler with either albuterol or a dummy drug at regular times four times a day. Then for the last nine months of the study, all subjects will be given the albuterol dry powder inhaler and will use it only when needed to help with breathing problems. Subjects will need to keep a daily diary (both paper and electronic) throughout the study recording any inhaler use and health problems. There will be visits to the study doctor about once a month for a year. This study is intended to show that the albuterol dry powder inhaler works well and is safe for use over a long period of time.

Study identification

NCT ID
NCT01218009
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
331 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
Oct 2010 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2010 (Actual)
Last update posted
May 20, 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 20, 2015 · Synced Oct 24, 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 NCT01218009 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →