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).

Launched by ASTRAZENECA · Sep 28, 2023

Keywords

ClinConnect Summary

This clinical trial is studying the effects of a new inhaler that combines three medications—Budesonide, Glycopyrronium, and Formoterol Fumarate—on exercise performance in people with Chronic Obstructive Pulmonary Disease (COPD). The study will compare this inhaler to another inhaler that has Budesonide and Formoterol Fumarate, as well as a placebo (a treatment with no active ingredients). The goal is to see how these treatments affect important breathing and exercise measurements.

To participate, you must be between 40 and 80 years old and have a confirmed diagnosis of moderate to severe COPD. You should also have been stable on your current COPD medication for at least six weeks and have a history of smoking. If you are interested in joining the study, you can expect to undergo a few tests to check your lung function and exercise capability. It's important to note that certain health conditions, like asthma or other serious respiratory diseases, could make you ineligible. This trial is currently recruiting participants, so if you think you might be a good fit, it could be a valuable opportunity to contribute to COPD research.

Gender

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Eligibility criteria

• Inclusion Criteria:
• • 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.
• Exclusion Criteria:
• • 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.