Study identifier:D5980R00093
ClinicalTrials.gov identifier:NCT07103642
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 Japan Study)
Pulmonary Disease, Chronic Obstructive
Phase 4
No
BGF
All
3402
Observational
40 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Aug 2025 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
PROMPT PATIENTS INITIATING BGF WITHIN 30-DAYS OF EXACERBATION | Drug: BGF BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL |
DELAYED PATIENTS INITIATING BGF WITHIN 31-180 DAYS OF EXACERBATION | Drug: BGF BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL |
VERY DELAYED PATIENTS INITIATING BGF BETWEEN 181 AND 365 DAYS AFTER EXACERBATION | Drug: BGF BUDESONIDE/GLYCOPYRRONIUM/FORMOTEROL |