Title
Efficacy and Safety of Levalbuterol Versus Racemic Albuterol in Asthma
A Randomized, Double-Blind Study to Determine the Efficacy of Levalbuterol Versus Racemic Albuterol in the Treatment of Acute Asthma
Phase
Phase 3Lead Sponsor
SunovionStudy Type
InterventionalStatus
Completed No Results PostedIndication/Condition
AsthmaIntervention/Treatment
albuterol levalbuterol ...Study Participants
627To investigate the Efficacy and Safety of Levalbuterol versus Racemic Albuterol in the Treatment of Acute Asthma.
This study is a double-blind, randomized, active-controlled, multicenter, parallel-group trial of levalbuterol in adult subjects with acute reversible airways disease. Approximately 600 subjects will be enrolled and study participation will consist of 2 periods: Period I (Acute Period): Double-blind treatment in the Emergency Department (ED) or Clinic until disposition, for a maximum of 24 hours of double-blind treatment and Period II (Post-Acute Period): Subjects discharged from the ED or Clinic will continue double blind treatment (with the same treatment provided as rescue medication as MDI) for approximately 10 days. Subjects will be contacted by telephone 30 days post discharge to assess relapse. This study was previously posted by Sepracor Inc. In October 2009, Sepracor Inc. was acquired by Dainippon Sumitomo Pharma., and in October 2010, Sepracor Inc's name was changed to Sunovion Pharmaceuticals Inc.
levalbuterol 1.25 mg Period I: administered every 20 minutes for the first 3 doses, and then every 40 minutes for the next 3 doses; then as clinically indicated. Period II: TID for 3 days (same time of day), then PRN to TID for 7 days
Racemic Albuterol 2.5 mg Period I: every 20 min for the first 3 doses, then every 40 min for the next 3 doses, then as clinically indicated. Period II: TID for 3 days then PRN to TID for 7 days
Inclusion Criteria: Male and female subjects must be at least greater than or equal to 18 years of age at the time of consent. Subjects must have history of asthma for at least 6 months. Subjects must present to the emergency department (ED) or clinic with forced expiratory volume in one second (FEV1) of 20 to 55% (inclusive) predicted at baseline Subjects must have O2 saturation greater than or equal to 90% at room air or with no more than 6 Liters/minute supplemental oxygen and no other cause of wheezing or shortness of breath other than asthma as determined by the physician. Prior use of a beta-agonist (e.g., Primatine Mist, albuterol, salmeterol, etc.) within 24 hours of presentation to the ED or Clinic. Smoked ≤ 10 pack-years or non-smoker. Be in good health with the exception of asthma and not suffering from any chronic condition which might affect their lung function, such as COPD or emphysema. Near-normal activity level between exacerbations. Subjects who are taking inhaled or systemic corticosteroids must be on a stable dose for at least 21 days prior to study entry. Exclusion Criteria: Subjects who have received treatment for asthma in an ED, Clinic, or Urgent Care Center within 2 weeks prior to study entry. Based upon history or physical exam in the ED or Clinic, subjects with known or suspected cause of pulmonary symptoms other than asthma, such as COPD, CHF, pneumonia, pulmonary embolism, or angioedema. Subjects with a history of asthma episodes associated with hypercapnia, respiratory arrest, hypoxic seizures, or requiring intubation within 12 months prior to entry. Hospitalization for asthma within two months prior to entry. Female subjects who are pregnant or lactating. Subjects who have a history of a clinically significant psychiatric disorder within the last 3 months, with the exception of mild depression. Subjects who have participated in an investigational drug study within 30 days of study entry or have previously participated in the current trial.
