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

PHASE3CompletedINTERVENTIONAL
Enrollment

117

Participants

Timeline

Start Date

February 28, 2001

Primary Completion Date

July 31, 2002

Study Completion Date

July 31, 2002

Conditions
Reactive Airways Disease (RAD)
Interventions
DRUG

Levalbuterol HCl Inhalation Solution

Nebulized unit dose vial for inhalation, low dose (0.15 mg, 0.31 mg or 0.63 mg), adjusted for body weight

DRUG

Levalbuterol HCl Inhalation Solution

Nebulized unit dose vial for inhalation, high dose (0.31 mg, 0.63 mg or 1.25 mg), adjusted for body weight

DRUG

Albuterol HCl Inhalation Solution

Nebulized unit dose vial for inhalation, dose (0.31 mg, 0.63 mg or 1.25 mg), adjusted for body weight

Trial Locations (34)

Unknown

Little Rock

Corona

Englewood

Huntington Beach

Long Beach

Sacramento

San Diego

Denver

Washington D.C.

Lake Worth

Tampa

Bloomington

Chicago

Indianapolis

Lexington

Louisville

Marrero

Shreveport

Omaha

New York

Raleigh

Winston-Salem

Cleveland

Columbus

Oswego

Medford

Dallas

Houston

San Antonio

Burke

Norfolk

Charleston

Halifax

Saskatoon

All Listed Sponsors
lead

Sumitomo Pharma America, Inc.

INDUSTRY

NCT00685126 - Study of Levalbuterol and Racemic Albuterol in Pediatric Subjects With Reactive Airways Disease (RAD) | Biotech Hunter | Biotech Hunter