Outcomes in Real-life After Initation of Treatment With Trixeo (Budesonide / Glycopyrronium / Formoterol)

CompletedOBSERVATIONAL
Enrollment

250

Participants

Timeline

Start Date

June 1, 2023

Primary Completion Date

May 31, 2025

Study Completion Date

May 31, 2025

Conditions
Chronic Obstructive Pulmonary Disease
Interventions
DRUG

BGF (budesonide/glycopyrrolate/formoterol fumarate)

BGF is a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease (COPD) who are not adequately treated by a combination of an ICS and a LABA, or a combination of a LABA and a LAMA. The decision to start treatment with BGF must be made by the treating physician according to the subjects' medical need and a positive benefit/risk balance. The decision to prescribe BGF must be independent of enrolment into the study, must be determined by the treating physician and should be taken according to the standard of current best medical practice and national guidelines.

Trial Locations (20)

Unknown

Research Site, Acquaviva delle Fonti

Research Site, Alessandria

Research Site, Ancona

Research Site, Avellino

Research Site, Brescia

Research Site, Brindisi

Research Site, Busto Arsizio (Varese)

Research Site, Catania

Research Site, Catanzaro

Research Site, Cittadella (Padova)

Research Site, Florence

Research Site, Foggia

Research Site, Lecce

Research Site, Napoli

Research Site, Passirana (Milano)

Research Site, Pavia

Research Site, Roma

Research Site, Torino

Research Site, Treviso

Research Site, Verona

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY