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ACTIVE NOT RECRUITINGN/A

Pooled Analysis of Single-arm Studies of Budesonide/Glycopyrronium/Formoterol (BGF) in Routine Care Setting

Sponsor: AstraZeneca

NCT ID: NCT06712563

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Budesonide/glycopyrrolate/formoterol fumarate (drug)
How long the study runs
Study runs about 20 months (dates as stated)
About the drug or intervention
Budesonide/glycopyrrolate/formoterol fumarate — drug: Budesonide/glycopyrrolate/formoterol fumarate (BGF) is a triple fixed-dose combination therapy for adults with moderate to severe COPD who are not adequately treated by a combination of inhaled corticosteroids and long-acting beta-agonist (LABA), or LABA and long-acting muscarinic-antagonist
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
2,000
Started
2025-04-17
Last checked
2026-07

Plain English Summary

What is this study?

  • • Testing a new treatment for pulmonary disease, chronic obstructive
  • • Clinical study - 2,000 participants
  • • The CHOROS pooled analysis is a retrospective secondary data use analysis of integrated individual participant data from a series of planned and on-going primary prospective, non-interventional, multi-center studies sponsored by AstraZeneca and conducted in the pulmonary/primary care practitioner setting in multiple countries and may include data from the following countries: United Kingdom, Germany, Italy, Greece, Japan, Canada and Romania

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with pulmonary disease, chronic obstructive

Where?

  • • London - Research Site

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The CHOROS pooled analysis is a retrospective secondary data use analysis of integrated individual participant data from a series of planned and on-going primary prospective, non-interventional, multi-center studies sponsored by AstraZeneca and conducted in the pulmonary/primary care practitioner setting in multiple countries and may include data from the following countries: United Kingdom, Germany, Italy, Greece, Japan, Canada and Romania.

Pulmonary Disease, Chronic Obstructive

How this trial compares with your answers

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What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Patients with moderate to severe COPD and initiating BGF treatment according to the local prescribing guidance and...
  • ✓Enrolled in on-going single-arm studies
  • ✓Provided consent for secondary use of data

Who cannot take part

  • ✗Did not provide consent for secondary use of data
See the full criteria
Inclusion Criteria: * Patients with moderate to severe COPD and initiating BGF treatment according to the local prescribing guidance and as per their treating physician's recommendation * Enrolled in on-going single-arm studies * Provided consent for secondary use of data Exclusion Criteria: * Did not provide consent for secondary use of data

Where Is This Study? (1 UK site)

Research Site

London, United Kingdom

Data sourced from ClinicalTrials.gov · Last verified: 2026-07