This is a randomized, double-blind, placebo-controlled, multicenter, parallel group study to compare 2 dose levels of BDA MDI (PT027) to its components BD MDI (PT008) and AS MDI (PT007) on improvement in lung function and asthma symptoms after 12 weeks of treatment in adult, adolescent, and child subjects with symptomatic asthma currently being treated with a short/rapid-acting 2-adrenoreceptor agonist (SABA; eg, Ventolin) as needed alone or with low-dose inhaled corticosteroid (ICS) maintenance therapy plus SABA as needed.
Condition | Asthma, Asthma, Asthma (Pediatric), Allergies & Asthma, Allergies & Asthma, Asthma (Pediatric), asthmatic, bronchial asthma |
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Treatment | Budesonide/albuterol sulfate metered-dose inhaler 80/180 μg, Budesonide/albuterol sulfate metered-dose inhaler 160/180 μg, Albuterol sulfate metered-dose inhaler 180 μg, Budesonide metered-dose inhaler 160 µg, Placebo metered-dose inhaler |
Clinical Study Identifier | NCT03847896 |
Sponsor | Bond Avillion 2 Development LP |
Last Modified on | 28 May 2022 |
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