A Study to Evaluate the Effect of Budesonide, Glycopyrronium, Formoterol Fumarate (BGF) Metered Dose Inhaler (MDI), Budesonide and Formoterol Fumarate (BFF) MDI and Placebo MDI on Exercise Parameters in Participants With Chronic Obstructive Pulmonary Disease (COPD).

Completed · Phase 3 · Has a placebo group

Conditions studied: Chronic Obstructive Pulmonary Disease

In brief

This study will investigate the effect of Budesonide, Glycopyrronium, and Formoterol Fumarate (BGF) metered dose inhaler (MDI) compared with Placebo MDI, and Budesonide and Formoterol Fumarate (BFF) MDI on isotime inspiratory capacity (IC) and exercise endurance time.

Key facts

Study ID: NCT06067828
Run by: AstraZeneca
People needed: 171
Starts: 2023-10-24
Expected to finish: 2026-01-22
Last updated by the study team: 2026-03-05

Who can join

Age: 40 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Participant must be male or female, 40 to 80 years of age inclusive, at the time of signing the informed consent.
Participant must have:
a diagnosis of COPD confirmed by a post-bronchodilator Forced expiratory volume (FEV1)/ Forced vital capacity (FVC) < 0.7 at Visit 1
a post-bronchodilator FEV1 ≥ 30% and <80% predicted normal (moderate to severe COPD) at Visit 1.
a score of ≥ 2 on the modified Medical Research Council at Visit 1.
pre-bronchodilator FRC of > 120% of predicted normal FRC values at Visit 1.
a constant work rate test endurance time of 3 to 8 minutes at Visit 2.
Participant must be on a stable dose of mono-or dual inhaled maintenance COPD treatment for at least 6 weeks.
Current or former smoker with a history of ≥ 10 pack-years of tobacco smoking
Body mass index < 40 kg/m2.
Male and Female participants (not applicable for female participants with non-childbearing potential) and their partners must use an acceptable method of contraception.

You may not qualify if…

A current diagnosis of asthma, asthma- COPD-overlap, or any other chronic respiratory disease other than COPD such as alpha-1 antitrypsin deficiency, active tuberculosis, lung cancer, lung fibrosis, sarcoidosis, interstitial lung disease and pulmonary hypertension.
Historical or current evidence of a clinically significant disease
Participants on oxygen therapy or that desaturate significantly (<82%) during exercise.
Participants who are enrolled or entering a pulmonary rehabilitation program during the study.
Participants who have cancer that has not been in complete remission for at least 5 years.
Participants with a diagnosis of narrow-angle glaucoma that has not been adequately treated and/or change in vision that may be relevant, in the opinion of the investigator.
Participants with symptomatic prostatic hypertrophy or bladder neck obstruction/urinary retention that, in the opinion of the investigator, is clinically significant.
Participants who have a history of hypersensitivity to β2-agonists, budesonide or any other corticosteroid components, glycopyrronium or other muscarinic anticholinergics, or any component of the MDI or dry powder inhaler.
Participant with resting (5 minutes) oxygen saturation SaO2 in room air ≤ 85%.
A COPD exacerbation that requires hospitalization within 12 months prior to Visit 1 or a COPD exacerbation that requires systemic corticosteroids or antibiotics within 4 months of Visit 1.
Participants with contraindications to cardiopulmonary exercise testing (CPET).
Participants who have had a respiratory tract infection within 8 weeks prior to Visit 1 and/or during the screening period.
Participants with lung lobectomy, lung volume reduction or lung transplantation.
Unable to withhold short-acting bronchodilators for 6 hours prior to lung function testing at each study visit.
Known history of drug or alcohol abuse within 12 months.
Any regular recreational use of marijuana in the 12 months.

Where it is running

Research Site — Hanover, Germany
Research Site — Heidelberg, Germany
Research Site — Lübeck, Germany
Research Site — Mainz, Germany
Research Site — Daegu, South Korea
Research Site — Seoul, South Korea
Research Site — Seoul, South Korea
Research Site — Benalmádena, Spain
Research Site — Madrid, Spain
Research Site — Santiago de Compostela, Spain
Research Site — Seville, Spain
Research Site — Leicester, United Kingdom
Research Site — London, United Kingdom
Research Site — London, United Kingdom
Research Site — Manchester, United Kingdom
Research Site — Los Angeles, California, United States
Research Site — Tarzana, California, United States
Research Site — Torrance, California, United States
Research Site — Brooksville, Florida, United States
Research Site — Anderson, South Carolina, United States
Research Site — Greenville, South Carolina, United States
Research Site — Spartanburg, South Carolina, United States
Research Site — Edmonton, Alberta, Canada
Research Site — Kingston, Ontario, Canada
Research Site — Sainte-Foy, Quebec, Canada

Full record on ClinicalTrials.gov

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