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Completed Phase 3 Interventional

Study of Levalbuterol and Racemic Albuterol in Pediatric Subjects With Reactive Airways Disease (RAD)

ClinicalTrials.gov ID: NCT00685126

Public ClinicalTrials.gov record NCT00685126. 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 Jun 26, 2026, 5:32 PM 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 Safety, Tolerability and Efficacy Study of Levalbuterol and Racemic Albuterol in Pediatric Subjects Birth to 48 Months Old With Reactive Airways Disease in an Acute Setting

Study identification

NCT ID
NCT00685126
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sumitomo Pharma America, Inc.
Industry
Enrollment
117 participants

Conditions and interventions

Interventions

  • Levalbuterol HCl Inhalation Solution Drug
  • Albuterol HCl Inhalation Solution Drug

Drug

Eligibility (public fields only)

Age range
Up to 48 Months
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
Jan 31, 2001
Primary completion
Jun 30, 2002
Completion
Jun 30, 2002
Last update posted
Feb 21, 2012

2001 – 2002

United States locations

U.S. sites
32
U.S. states
17
U.S. cities
32
Facility City State ZIP Site status
Not listed Little Rock Arkansas
Not listed Corona California
Not listed Englewood California
Not listed Huntington Beach California
Not listed Long Beach California
Not listed Sacramento California
Not listed San Diego California
Not listed Denver Colorado
Not listed Washington D.C. District of Columbia
Not listed Lake Worth Florida
Not listed Tampa Florida
Not listed Bloomington Illinois
Not listed Chicago Illinois
Not listed Indianapolis Indiana
Not listed Lexington Kentucky
Not listed Louisville Kentucky
Not listed Marrero Louisiana
Not listed Shreveport Louisiana
Not listed Omaha Nebraska
Not listed New York New York
Not listed Raleigh North Carolina
Not listed Winston-Salem North Carolina
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Oswego Ohio
Not listed Medford Oregon
Not listed Dallas Texas
Not listed Houston Texas
Not listed San Antonio Texas
Not listed Burke Virginia
Not listed Norfolk Virginia
Not listed Charleston West Virginia

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00685126, 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 Feb 21, 2012 · Synced Jun 26, 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 protocol, eligibility criteria, and contact information for NCT00685126 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →