Budesonide Glycopyrronium bromide Formoterol fumarate pressurized Metered Dose Inhaler
Combination ProductParticipants with moderate to severe Chronic Obstructive Pulmonary Disease
NCT Number: NCT05915182
Chronic obstructive pulmonary disease (COPD) is a debilitating and progressive respiratory condition characterized by irreversible airflow limitation. The overall 5-year survival for COPD patients is 56-92%, depending on disease severity. Considering the recent introduction of the Budesonide, Glycopyrronium bromide and Formoterol fumarate Metered-Dose Inhaler (BGF MDI) in COPD therapeutic arsenal as well as the increasingly important role of real-world (RW) data in health care decisions, as it bridges gaps not addressed by randomized clinical trials, there is a need for RW evidence studies that can serve as inputs for Health Technology Assessment (HTA) submissions. In view of this need, this study is designed to generate RW evidence on the clinical and patient-reported outcomes of treatment with BGF MDI over a 52-week treatment period in routine care settings in Greece as well as to shed light on the reasons for switching from dual to triple therapy with BGF MDI, aiming at further characterizing the multifactorial aspects of inadequate COPD management that lead physicians to step-up treatment. The study is mainly descriptive in nature and is not planned to reject or affirm any formal statistical hypothesis. This is a single-country, non-interventional, multicenter, 52-week prospective cohort study, mainly based on primary data collection, which will include adult patients with moderate to severe COPD newly prescribed maintenance treatment with BGF MDI in routine care settings of Greece. This study design has been selected on the basis that such studies essentially, through collecting data generated in the course of routine clinical care about management practices and their outcomes from both the physician and patient perspective, help to bridge the knowledge gap between clinical research in controlled randomized settings and daily clinical practice. In line with the purely observational and non-interventional nature of the study, no changes to the current standard of care will be required and all aspects of treatment and clinical management of patients will be in accordance with local clinical practice and at the discretion of the participating physicians. The conduct of this study will adhere to the applicable national regulatory requirements governing the conduct of such type of clinical research. In addition, the study has been designed and will be conducted and reported in accordance with the ethical principles laid down in the Declaration of Helsinki, the Guidelines for Good Pharmacoepidemiology Practice (GPP) of the International Society for Pharmacoepidemiology, the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines where applicable, the European Union (EU) General Data Protection Regulation (GDPR), and the local rules and regulations. Patients will have been prescribed BGF MDI (Trixeo Aerosphere™) prior to informed consent (IC) obtainment and will be treated according to the local prescribing information (Summary of Product Characteristics [SmPC]) of the study medication and routine medical practice in terms of visit frequency and type of assessments performed. The assignment of the patient to this therapeutic strategy is not decided in advance by the study protocol but falls within current practice and the prescription of BGF MDI is clearly separated from the physician's decision to include the patient in the current study. In addition, every medical decision including the course of treatment will reflect exclusively the decision of the treating physician in a routine clinical situation according to the product's SmPC. Follow-up visit frequency will be determined by the treating physician, however study-related data will be collected at study enrollment and at 12, 24, 36, and 52-week data collection timepoints post-index (i.e., after BGF MDI treatment initiation) with an allowable time window of ±2 weeks for each data collection timepoint. Data collection at the aforementioned timepoints will be performed in the context of on-site routine visits at the private practices/hospital clinics. In addition, a telephone contact will take place at 4 (±1) weeks post-index for the sole purpose of administering COPD Assessment Test (CAT) by phone interview with the patient. Any visits/contacts occurring at other times not pre-planned in the context of the study will not be captured for the purposes of this study, except for safety-related information, exacerbation data, information on BGF MDI and concomitant COPD-related treatments, that will be collected on a continuous basis. Data collection at all indicated timepoints will be performed in the context of on-site routine visits at the private practices/hospital clinics. There are no dose regimens or diagnostic procedures pre-defined within this study plan. Participation in this observational, real-life study and its documentation procedure will not affect the routine treatment situation in any way.
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Notify Me40 year–80 year
All sexes
Observational
Research Site, Alexandroupoli, Greece
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants with moderate to severe Chronic Obstructive Pulmonary Disease
Time frame: At 12 weeks after treatment initiation
Assess the change in Chronic Obstructive Pulmonary Disease (COPD) health status measured by the COPD Assessment Test (CAT) in COPD patients initiated on Budesonide, Glycopyrronium bromide, Formoterol fumarate Metered Dose (BGF MDI) Inhaler after 12 weeks of treatment
Time frame: At 12 weeks after treatment initiation
Estimate the proportion of CAT responders among COPD patients initiated on Budesonide, Glycopyrronium bromide, Formoterol fumarate Metered Dose (BGF MDI) Inhaler after 12 weeks of treatment
Time frame: At treatment initiation timepoint
To describe and count in numbers the reasons for switch from dual LAMA/LABA or ICS/LABA to single-inhaler triple combination therapy with BGF MDI
Time frame: At 4, 24, 36, 52 weeks after treatment initiation
To assess the change in COPD health status measured by the CAT among COPD patients initiated on BGF MDI after 4, 24, 36, and 52 weeks of treatment
Time frame: At 4, 24, 36, 52 weeks after treatment initiation
To estimate the proportion of CAT responders among COPD patients initiated on BGF MDI after 4, 24, 36, and 52 weeks of treatment
Time frame: At 12, 52 weeks after treatment initiation
To assess the change in HRQoL measured by the SGRQ-C on the overall study population, after 12 and 52 weeks of treatment
Time frame: At 12, 52 weeks after treatment initiation
To assess the change in HRQoL measured by the SGRQ-C to estimate the proportion of SGRQ-C responders among COPD patients initiated on BGF MDI after 12 and 52 weeks of treatment.
Time frame: At treatment initiation timepoint
To assess the severity of dyspnea at baseline measured by the baseline dyspnea index (BDI)
Time frame: At 12, 52 weeks after treatment initiation
To estimate the change in dyspnea severity (measured by the TDI) on the overall study population after 12 and 52 weeks of treatment.
Time frame: At 12, 52 weeks after treatment initiation
To estimate the proportion of TDI responders among COPD patients initiated on BGF MDI after 12 and 52 weeks of treatment
Time frame: At 12, 24, 36, 52 weeks after treatment initiation
To assess the change in spirometric lung function as measured by FEV1 on the overall study population after 12, 24, 36, and 52 weeks of treatment
Time frame: At 12, 24, 36, 52 weeks after treatment initiation
To estimate the proportion of FEV1 responders among COPD patients initiated on BGF MDI after 12, 24, 36, and 52 weeks of treatment
Time frame: At 12 weeks after treatment initiation
To determine the Early Clinically Important Improvement (ECII) rate in COPD patients initiated on BGF MDI after 12 weeks of treatment
Time frame: At 52 weeks after treatment initiation
To assess the CII rate after 52 weeks of treatment among the 12-week ECII responders
Time frame: At treatment initiation timepoint
To describe the number of moderate and severe exacerbations during the 52 week period prior to BGF MDI initiation
Time frame: During 52 weeks after treatment initiation
To describe the number of moderate and severe exacerbations during the 52-week period after BGF MDI initiation
Time frame: At 52 weeks after treatment initiation
To assess the overall treatment response rate based on lung function, PROs and exacerbation rate after 52 weeks of treatment with BGF MDI
Time frame: At 52 weeks after treatment initiation
To assess the response rates based on individual measures of lung function, PROs, and exacerbation rate after 52 weeks of treatment with BGF MDI
Time frame: At 12 weeks after treatment initiation
To evaluate the treatment satisfaction, assessed by the Treatment Satisfaction Questionnaire for Medication (TSQM vII) after 12 of treatment with BGF MDI
Time frame: At 52 weeks after treatment initiation
To evaluate the treatment satisfaction, assessed by the Treatment Satisfaction Questionnaire for Medication (TSQM vII) after 52 weeks of treatment with BGF MDI
Time frame: At 52 weeks after treatment initiation
To assess the patient-reported overall change in health status since the start of treatment with BGF MDI, using the Patient Global Impression of Change (PGIC) questionnaire
Time frame: At 12, 24, 36, 52 weeks after treatment initiation
To assess the patient-reported overall global impression of severity after 12, 24, 36, and 52 weeks of treatment with BGF MDI, using the Patient Global Impression of Severity (PGIS) questionnaire
Time frame: At 12, 24, 36, 52 weeks after treatment initiation
To assess patients' adherence to treatment with BGF MDI, using the Medication Adherence Report Scale (MARS-5), after 12, 24, 36, and 52 weeks of treatment
Time frame: At 12, 24, 36, 52 weeks after treatment initiation
To assess the number of patients completely and not completely adherent at 12, 24, 36 and 52 weeks post-index
Time frame: At 52 weeks after treatment initiation
To assess number of patients remaining on treatment at 52-weeks of treatment
Time frame: At 52 weeks after treatment initiation
To assess the number of patients having discontinued treatment at 52 weeks of treatment
Time frame: During 52 weeks after treatment initiation
To assess the time from the start of BGF MDI to all cause treatment discontinuation
AstraZeneca
Industry
A Real-world, Multicenter, 52-week Prospective Cohort Study to Capture the Reasons for Switch to Triple Combination Therapy and to Assess the Clinical and Patient Reported Outcomes in Adults With Moderate to Severe COPD Treated With Trixeo Aerosphere™ in Routine Care Settings in Greece.
Acronym: TRIAENA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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