Budesonide/formoterol fumarate dihydrate versus budesonide with a novel suspension technology for uncontrolled asthma: phase 3 VATHOS study.
Abstract
Background: ). Methods: , 5 min post-dose) and severe exacerbation rates (secondary). Adverse events (AEs) were recorded. Results: in lung function. Conclusion: 320 with co-suspension delivery technology in people with inadequately controlled asthma on medium-dose ICS or ICS/LABA.
Fields of Study & Subjects
Asthma and respiratory diseases
Inhalation and Respiratory Drug Delivery
Respiratory and Cough-Related Research
Publication details
- Journal / source
- PubMed
- Publisher
- European Respiratory Society (ERS)
- Volume
- 12
- Issue
- 5
- Pages
- 01817-2025
- Publication date
- 1 September 2026
- Language
- EN