A Safety, Efficacy and Tolerability Study in Pediatric Subjects With Asthma

Completed · Phase 3 · Has a placebo group

Conditions studied: Asthma

In brief

A Safety, Efficacy, and Tolerability Study of Daily Dosing with Levalbuterol Tartrate HFA MDI and Placebo in Subjects Aged Birth to \<48 Months with Asthma.

Key facts

Study ID

NCT00809757

Run by

Sumitomo Pharma America, Inc.

People needed

197

Starts

2008-12-01

Expected to finish

2013-06-01

Last updated by the study team

2014-07-28

Who can join

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

You may qualify if…

• Subject's parent/legal guardian must give written informed consent, including privacy authorization, prior to study participation. Complete documentation regarding the consent process must be recorded in the case report form (CRF) and source documentation.
• Subject's parent/legal guardian must be willing and able to comply with the study procedures and visit schedules.
• Subject, male or female, must be between the ages of birth and <48 months, exclusive, at the time of consent.
• Subjects 24 to <48 months of age must have a history of physician-diagnosed asthma (defined as at least 3 episodes of respiratory symptoms consistent with asthma symptoms including, but not limited to, cough, wheeze, or dyspnea).
• Subjects 0 to <24 months of age must have a history of 3 episodes of respiratory symptoms that in the judgement of the investigator could be consistent with asthma or reactive airways disease.
• Subject must be in good health and not affected by any other chronic conditions, including respiratory disorders other than asthma.
• In subjects with a chest radiograph (taken 12 months prior to screening visit), no evidence of any chronic cardiopulmonary condition other than asthma should be present as discerned by the Investigator.
• Subject's parent/legal guardian must be able to complete the diary cards and medical event calendars (MEC) reliably on a daily basis and understand dosing instructions and questionnaire completion.

You may not qualify if…

• Subject who requires or is expected to require any disallowed medications
• Subject who has participated in an investigational drug study within 30 days prior to screening, or who is currently participating in another clinical trial.
• Subject or parent/legal guardian who has daily commitments during the study that would interfere with trial measurements, compliance, or both.
• Subject who has a history of hospitalization for asthma, reactive airways disease, or bronchospasm within 4 weeks prior to screening or who is scheduled for in-patient hospitalization, including elective surgery during the course of the trial.
• Subject who has experienced significant blood loss within 60 days of study drug.
• Subject with a clinical diagnosis of cystic fibrosis.
• Subject who was born prematurely, defined as less than 38 weeks gestational age at birth, and is <1 year of age at screening
• Subject whose body weight is less than 7.0 kg at screening. This minimum weight requirement is based upon standard pediatric growth charts [CDC 2000].
• Subject with a known sensitivity to levalbuterol or racemic albuterol, or any of the excipients contained in any of these formulations.
• Subject using any prescription drug with which levalbuterol or racemic albuterol sulfate administration is contraindicated.
• Subject with a history of life-threatening asthma, defined as previous asthma episodes requiring intubation or associated with hypercapnia, respiratory arrest, or hypoxic seizures.
• Subject with clinically significant abnormalities that may interfere with the metabolism or excretion of the study drugs or study participation (eg, abnormalities of renal, hepatic, metabolic, or endocrine function).
• Subject with a history of cancer.
• Subject with any chronic or congenital cardiorespiratory condition other than asthma including, but not limited to, bronchopulmonary dysplasia, congenital heart disease, and cystic fibrosis.
• Subject affected by an upper or lower respiratory tract infection in the 3 weeks prior to screening.
• Subject with a history of ventilation for a respiratory condition occurring at or near birth, including those associated with prematurity or bronchopulmonary dysplasia. Ventilatory support for elective non-cardiopulmonary surgery is not exclusionary. - Subject with any clinically significant abnormal laboratory values (hematology, blood chemistry).
• Subject with a clinically significant abnormal 12-lead ECG that would put the subject at risk for experiencing adverse cardiac effects.
• Subject who is a relative of a staff member.

Where it is running

• Little Rock Allergy & Asthma Clinical Research Center — Little Rock, Arkansas, United States
• West Coast Clinical Trials, LLC — Cypress, California, United States
• Allergy & Asthma Care Center of Southern California — Long Beach, California, United States
• Clinical Trials of Orange County, Inc. — Orange, California, United States
• Allergy and Asthma Consultants — Redwood City, California, United States
• IMMUNOe International Research Centers — Centennial, Colorado, United States
• All Seasons Allergy and Asthma Center, P.A. — Fort Walton Beach, Florida, United States
• Palm Beach Research Center — West Palm Beach, Florida, United States
• Brookstone Centre Parkway — Columbus, Georgia, United States
• Rush University Medical Center — Chicago, Illinois, United States
• Northern Illinois Research Associates — DeKalb, Illinois, United States
• Sneeze, Wheeze & Itch Associates LLC — Normal, Illinois, United States
• Nassim, McMonigle, Mescia & Associates — New Albany, Indiana, United States
• Grand Blanc Medical — Grand Blanc, Michigan, United States
• Craig A. Spiegel MD — Bridgeton, Missouri, United States
• Midwest Allergy and Asthma center — Omaha, Nebraska, United States
• The Asthma & Allergy Center, P.C. — Papillion, Nebraska, United States
• Maimonides Medical Center — Brooklyn, New York, United States
• St. Elizabeth Health Center — Utica, New York, United States
• Cincinnati Children's Hospital Medical Center — Cincinnati, Ohio, United States
• Dayton Clinical Research — Dayton, Ohio, United States
• Allergy, Asthma and clinical Research Center — Oklahoma City, Oklahoma, United States
• Eminence Research, LLC — Oklahoma City, Oklahoma, United States
• Asthma and Allergy Research Associates — Upland, Pennsylvania, United States
• National Allergy, Asthma, and Uticaria Centers — Charleston, South Carolina, United States

Full record on ClinicalTrials.gov

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