Resumen

Este estudio evaluará el efecto de la terapia triple ICS/LAMA/LABA con BGF IDM 320/14,4/9,6 μg sobre los desenlaces cardiopulmonares en comparación con la terapia LAMA/LABA con GFF IDM 14,4/9,6 μg en una población con EPOC y riesgo cardiopulmonar elevado.

Descripción detallada

Este es un estudio de fase III, aleatorizado, doble ciego, en grupos paralelos, multicéntrico, multinacional, impulsado por eventos, que compara BGF IDM 320/14,4/9,6 μg BID con GFF IDM 14,4/9,6 μg BID en participantes con EPOC que presentan riesgo de un evento cardiopulmonar.

Elegibilidad

Edad mínima: 40 YearsEdad máxima: 80 YearsSexo: ALL

Criterios de inclusión

Male or female participants must be 40 to 80 years of age inclusive, at the time of signing
the ICF.
Demonstrate acceptable MDI administration technique at Visit 1 (V1) and Visit 2 (V2)
A diagnosis of COPD confirmed by a post-bronchodilator FEV1/FVC ratio \< 70%
at V1.
Current or former smokers with a history of at least 10 pack-years of cigarette smoking;
defined as (number of cigarettes per day/20) x number of years smoked. Previous smokers are defined as those who have stopped smoking for at least 6
months prior to V1.
A baseline peripheral blood eosinophil count of ≥ 100 cells/mm3 assessed at Visit 1 by
the central laboratory
A CAT score of ≥ 10 at Visit 1.
Participant must fulfill at least 1 of the 4 CV disease/risk factor criteria below \[(a), (b),
(c), or (d)\]:
: Established CV Disease
: Combination of CV risk factors:
Hypertension
Diabetes Mellitus
Chronic Kidney Disease
Dyslipidemia
Obesity
: High risk of CV disease determined using an established CV risk assessment
tool.
: CT coronary Artery Calcification
Willing and, in the opinion of the investigator, able to adjust current COPD therapy, as
required by the protocol.
Willing to visit at the study site or participate in virtual visits as required per the protocol
to complete all study assessments.
A female is eligible to enter and participate in the study if the female is of:
Non-childbearing potential: either permanently sterilized or who are post-menopausal.
Childbearing potential: has a negative serum pregnancy test at V1 and must use one
highly effective form of birth control.
Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICF and in the protocol.

Criterios de exclusión

Active diagnosis of asthma within the past 5 years (previous diagnosis as a child or adolescent are eligible), asthma-COPD overlap, or any other chronic respiratory disease other than COPD such as alpha-1 antitrypsin deficiency, active tuberculosis, lung fibrosis, sarcoidosis, interstitial lung disease, and pulmonary hypertension.
End-stage renal disease requiring renal replacement therapy
History of heart or lung transplant or actively listed for heart or lung transplant.
Implanted left ventricular assist device or implant anticipated in \< 3 months.
History of lung cancer and/or treatment for lung cancer within the 5 years prior to Visit 1.
Unstable or life-threatening cardiac disease - participants with any of the following at Visit 1 would be excluded:
An MI or unstable angina in the last 8 weeks
Unstable or life-threatening cardiac arrhythmia requiring intervention in the last 8 weeks.
NOTE: Any participant who experiences unstable or life-threatening cardiac disease during the run-in period will be excluded but can be rescreened 8 weeks after the resolution of the event.
Pneumonia and/or moderate or severe COPD exacerbation that has not resolved at least 8 weeks prior to Visit 1
Any life-threatening condition, including malignancy, with a life expectancy \< 5 years, other than CV disease or COPD, that might prevent the participant from completing the study.
Use of maintenance ICS treatment within the past 12 months.
Unable to abstain from protocol-defined prohibited medications
Participation in another clinical study with a study intervention administered in the last 30 days or 5 half-lives, whichever is longer prior to Visit 1 (any other investigational product that is not identified in protocol is prohibited for use during the duration of the study).
Participants with a known hypersensitivity to LAMA, LABA or ICS or any component of the MDI.
Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site).
Judgment by the investigator that the participant should not participate in the study if the participant is unlikely to comply with study procedures, restrictions, and requirements.
Previous randomization in the present study.
For females only - currently pregnant (confirmed with positive pregnancy test) or breastfeeding

Ubicaciones

Research Site

Buenos Aires, Argentina

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Research Site

Buenos Aires, Argentina

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Research Site

Buenos Aires, Argentina

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Research Site

CABA, Argentina

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Research Site

Capital Federal, Argentina

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Research Site

Ciudad de Buenos Aires, Argentina

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Research Site

Ciudad de Buenos Aires, Argentina

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Research Site

Florida, Argentina

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Mar del Plata, Argentina

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Mendoza, Argentina

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Ranelagh, Argentina

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Rosario, Argentina

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Research Site

San Fernando, Argentina

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Research Site

San Juan Bautista, Argentina

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Research Site

San Miguel de Tucumán, Argentina

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Research Site

San Miguel de Tucumán, Argentina

RECRUITING

Resumen

Descripción detallada

Elegibilidad

Criterios de inclusión

Criterios de exclusión

Intervenciones

BGF MDI 320/14.4/9.6 μg

GFF MDI 14.4/9.6 μg

Ubicaciones

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Patrocinadores

Contactos

AstraZeneca Clinical Study Information Center