Albuterol HFA MDI in Pediatric Participants With Asthma

Completed · Phase 3 · Has a placebo group

Conditions studied: Asthma

In brief

The primary objective of this study is to evaluate the chronic-dose and efficacy of Albuterol-HFA-MDI relative to placebo in pediatric asthmatics.

Key facts

Study ID

NCT00577655

Run by

Teva Branded Pharmaceutical Products R&D, Inc.

People needed

103

Starts

2007-08-01

Expected to finish

2008-07-01

Last updated by the study team

2021-11-12

Who can join

Age: 4 and older, up to 11. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and female child aged 4-11 years, inclusive Asthma of a minimum of six months duration that has been stable for at least four weeks prior to screening.

You may not qualify if…

• Hospitalization for acute asthma exacerbation greater than two years in 12 months prior to screening and/or received ER treatment or hospitalization for asthma exacerbation.

Where it is running

• Pediatric Care Medical Group, Inc. — Huntington Beach, California, United States
• California Allergy & Asthma Medical Group — Palmdale, California, United States
• Center for Clinical Trials, LLC — Paramount, California, United States
• Integrated Research Group, Inc — Riverside, California, United States
• Center for Clinical Trials of Sacramento — Sacramento, California, United States
• Carlos Piniella, MD — Miami, Florida, United States
• Sneeze, Wheeze & Itch Associates, Inc. — Normal, Illinois, United States
• Asthma & Allergy Associates, PC — Elmira, New York, United States
• ENT & Allergy Associates — Newburgh, New York, United States
• St. Elizabeth's Children Health Center — Utica, New York, United States
• Regional Allergy & Asthma Consultants — Asheville, North Carolina, United States
• Clinical Research Institute of Southern Oregan, PC — Medford, Oregon, United States
• Virginia Adult & Pediatric Allergy & Asthma — Richmond, Virginia, United States

Full record on ClinicalTrials.gov

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