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.
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
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
Where Is This Study? (1 UK site)
Research Site
London, United Kingdom
