A retrospective real-world data study, assessing the relationship between the timing of Budesonide/Glycopyrrolate/Formoterol initiation following an exacerbation and the occurrence of subsequent exacerbations, severe cardiopulmonary events and other real-world outcomes in the United States
Study Type
OBSERVATIONAL
Enrollment
13,000
BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL
AstraZeneca
Wilmington, Delaware, United States
Annualized COPD Exacerbation Event Rate
Annualized rates of COPD exacerbation events observed from index date (qualifying exacerbation event) through study completion (or until end of data availability; mean follow-up 462 days
Time frame: Annualized rates from index exacerbation through end of data availability, mean follow-up 462 days
Annualized Cardiopulmonary Event Rate
Annualized rates of cardiopulmonary events observed from index date (qualifying exacerbation event) through study completion (until end of data availability)
Time frame: Annualized rates from index exacerbation through end of data availability; mean follow-up 462 days
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