Pharmacodynamic Bioequivalence of Metered Dose Inhalers of Albuterol Sulfate in Patients With Stable Mild Asthma

Completed · Phase 3 · Has a placebo group

Conditions studied: Bronchial Asthma

In brief

The purpose of this study is to demonstrate the pharmacodynamic bioequivalence of the test product to the reference product, using bronchoprovocation (methacholine challenge testing) in adult patients with stable mild asthma.

Key facts

Study ID

NCT02624505

Run by

Cipla Ltd.

People needed

110

Starts

2015-12-01

Expected to finish

2016-11-01

Last updated by the study team

2019-07-25

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male and non-pregnant female subjects (18-65 years of age)
• Forced Expiratory Volume in 1 second (FEV1) ≥ 80% of predicted. Airway responsiveness to methacholine demonstrated by a pre-albuterol dose (baseline) PC20 ≤ 8 mg/ml.
• Stable mild asthmatics based on National Asthma Education and Prevention Program (NAEPP) guidelines.
• Nonsmokers for at least 6 months prior to the study and a maximum smoking history of five pack-years (the equivalent of one pack per day for five years).
• Written informed consent.

You may not qualify if…

• Conditions which could alter airway reactivity to methacholine (e.g., pneumonia, upper respiratory tract infection, viral bronchitis and/or sinobronchitis) within six weeks prior to the screening visit.
• History of seasonal asthma exacerbations, in which case the patient should be studied outside of the relevant allergen season.
• History of a clinically significant disease or abnormality including congestive heart failure, uncontrolled hypertension, uncontrolled coronary artery disease, myocardial infarction, or cardiac dysrhythmia.
• History of cystic fibrosis, bronchiectasis or other respiratory diseases other than Asthma
• Historical or current evidence of significant hematologic, hepatic, neurologic, psychiatric, renal, or other diseases
• Known intolerance or hypersensitivity or hypersensitivity to any component of the albuterol metered dose inhaler (MDI).

Where it is running

• Colorado Allergy and Asthma Centers — Denver, Colorado, United States

Full record on ClinicalTrials.gov

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