Study identifier:D5980R00095
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
EXACERBATIONS AND REAL-WORLD OUTOMES INCLUDING CARDIOPULMONARY EVENTS AMONG PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE INITIATING BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL (MITOS: EROS+CP US Study)
Pulmonary Disease, Chronic Obstructive
Phase 4
No
BGF
All
13000
Observational
40 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Oct 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Prompt PATIENTS INITIATING BGF WITHIN 30-DAYS OF EXACERBATION | Drug: BGF BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL Other Name: BREZTRI |
DELAYED PATIENTS INITIATING BGF WITHIN 31-180 DAYS OF EXACERBATION | Drug: BGF BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL Other Name: BREZTRI |
VERY DELAYED PATIENTS INITIATING BGF WITHIN 181-365 DAYS OF EXACERBATION | Drug: BGF BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL Other Name: BREZTRI |