Assessment of the Safety, Efficacy, PK, and Extrapulmonary Pharmacodynamics (PD) of Albuterol Sulfate Pressurized Inhalation Suspension (Hereafter Referred to as AS MDI) Compared to Proventil as an Active Control in Subjects With Asthma

Completed · Phase 2

Conditions studied: Asthma

In brief

This is a randomized, cumulative dose, open-label, 2-period crossover, multi-center study to assess the safety, efficacy, PK, and extrapulmonary PD of cumulative doses of AS MDI compared to cumulative doses of Proventil as an active control in subjects with mild to moderate asthma

Key facts

Study ID

NCT03371459

Run by

AstraZeneca

People needed

46

Starts

2017-12-29

Expected to finish

2018-03-26

Last updated by the study team

2019-07-23

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Have stable (for 6 months) physician-diagnosed asthma with historical documentation of the diagnosis
• Must be receiving 1 of the following required inhaled asthma therapies listed below for at least the last 30 days; Only SABA, which is used as needed for rescue, or Low to medium doses of ICS (alone or in combination with LABA), used regularly as maintenance asthma therapy
• Demonstrate acceptable spirometry performance (ie, meet American Thoracic Society [ATS]/European Respiratory Society [ERS] acceptability/repeatability criteria
• Pre-bronchodilator FEV1 of ≥50 to <80% predicted normal value after withholding SABA ≥6 hours
• Confirmed FEV1 reversibility to Ventolin, defined as a post-Ventolin increase in FEV1 of ≥15%
• Only 2 reversibility testing attempts are allowed

You may not qualify if…

• Chronic obstructive pulmonary disease or other significant lung disease (eg, chronic bronchitis, emphysema, bronchiectasis with the need of treatment, cystic fibrosis, or bronchopulmonary dysplasia)
• Oral corticosteroid use (any dose) within 6 weeks
• Received any marketed (eg, omalizumab, mepolizumab, reslizumab) or investigational biologic within 3 months or 5 half-lives, whichever is longer, or any other medication specifically prohibited by the protocol
• Current smokers, former smokers with >10 pack-years history, or former smokers who stopped smoking <6 months (including all forms of tobacco, e-cigarettes [vaping], and marijuana)
• Life-threatening asthma as defined as any history of significant asthma episode(s) requiring intubation associated with hypercapnia, respiratory arrest, hypoxic seizures, or asthma-related syncopal episode(s)
• Historical or current evidence of a clinically significant disease
• Cancer not in complete remission for at least 5 years
• Hospitalized for psychiatric disorder or attempted suicide within 1 year
• Unable to abstain from protocol-defined prohibited medications during the study

Where it is running

• Research Site — Winter Park, Florida, United States
• Research Site — North Dartmouth, Massachusetts, United States
• Research Site — St Louis, Missouri, United States
• Research Site — Raleigh, North Carolina, United States
• Research Site — Medford, Oregon, United States

Full record on ClinicalTrials.gov

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