Study identifier:D5980R00121
ClinicalTrials.gov identifier:NCT07414134
EudraCT identifier:N/A
CTIS identifier:N/A
Exacerbations and Real-World Outcomes Among Patients with Chronic Obstructive Pulmonary Disease Following Severe Exacerbation (MITOS:EROS+DISCHARGE)
Chronic Obstructive Pulmonary Disease
N/A
No
BGF- BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL
All
3598
Observational
40 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Feb 2026 by AstraZeneca
AstraZeneca
-
No locations available
| Arms | Assigned Interventions |
|---|---|
| Prompt Patients initiating BGF within 30-days of exacerbation | Drug: BGF- BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL This is a real-world observational study evaluating the timing of BGF, post discharge. |
| Delayed Patients initiating BGF within 31-180 days of exacerbation | Drug: BGF- BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL This is a real-world observational study evaluating the timing of BGF, post discharge. |