Evaluate the Effect of Aclidinium Bromide on Long-term Cardiovascular Safety and Exacerbations in Moderate to Very Severe COPD Patients.

Chronic Obstructive Pulmonary Disease Clinical Trial

— ASCENT COPD  

Official title:

Double-blind, Randomized, Placebo-controlled, Parallel-group, Phase IV Study to Evaluate the Effect of Aclidinium Bromide on Long-term Cardiovascular Safety and COPD Exacerbations in Patients With Moderate to Very Severe COPD (ASCENT COPD)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01966107
• Other study ID #: D6560C00002
• Secondary ID: LAS-MD-45
• Status: Completed
• Phase: Phase 4
• Start date: October 16, 2013
• Est. completion date: September 21, 2017

Study information

• Verified date: November 2018
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The Objectives of this study are to assess the safety of Aclidinium bromide on major adverse cardiovascular events (MACE), to assess the overall safety of Aclidinium bromide and to assess whether Aclidinium bromide reduces moderate or severe COPD exacerbations. This study is a double-blind, randomized, placebo controlled, parallel-group study to evaluate the effect of Aclidinium bromide on the cardiovascular safety and COPD exacerbations in patients with moderate to very severe COPD, as defined by the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3635
• Est. completion date: September 21, 2017
• Est. primary completion date: September 21, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 130 Years

Eligibility

Inclusion Criteria:

• 1. Male or female outpatients = 40 years of age

• 2. Current or former cigarette smokers with a smoking history of at least 10 pack-years

• 3. A diagnosis of stable, moderate to very severe COPD (GOLD, 2015) with a post-bronchodilator FEV < 80% FEV1/forced vital capacity (FVC) ratio < 70%

• 4. Must have at least one of the following 4 criteria:

1. Documented cerebrovascular disease (stroke or transient ischemic attack, carotid stenosis)

2. Documented coronary artery disease (angina, MI, angioplasty/stent/bypass)

3. Documented peripheral vascular disease or history of claudication

4. At least 2 of the following atherothrombotic risk factors as determined by the PI:

1. Male = 65 years or female = 70 years

2. Diabetes

3. Dyslipidemia

4. Hypertension

5. Waist circumference inches males = 40 in or in females = 38 inches

6. Evidence of renal dysfunction (eGFR < 60) and microalbuminuria (eGFR is based on modification of diet in renal disease [MDRD] equation, microalbuminuria is defined as = 30-300 mcg/mg creatinine on a spot urine or =30 mg creatinine on a 24hr urine test)

• 5. Maintained stable respiratory medications for 2 weeks prior to randomization (Appendix II)

• 6. Able to perform pulmonary function test (PFT) maneuvers and follow study procedures

• 7. Women of childbearing potential must have a negative serum ß-human chorionic gonadotropin (HCG) pregnancy test at Visit 1A and be practicing medically acceptable method of contraception. Otherwise, female patients should be at least 1 year postmenopausal, surgically sterile (defined as having a hysterectomy or tubal ligation).

• 8. Should understand study procedures and be willing to participate in the study as indicated by signing the ICF

Exclusion Criteria:

• 1. Significant diseases other than COPD or cardiovascular disease (e.g., metastatic cancer) which, in the opinion of the PI, may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study

• 2. Unstable or life threatening cardiovascular disease or COPD as determined by the PI

• 3. Patients with comorbid lung disease such as asthma, cystic fibrosis, bronchiectasis, interstitial lung disease, or pulmonary thromboembolic disease

• 4. Planned lung transplant or lung volume reduction surgery

• 5. Currently treated with a combination of LAMA and LABA/ICS therapy.

• 6. Malignancy for which patient has undergone resection, radiation therapy or chemotherapy within 5 years prior to screening. Patients with treated basal cell and squamous cell (skin) carcinoma are allowed

• 7. Respiratory infection or COPD exacerbation at Screening and/or within 4 weeks prior to screening

• 8. Uncontrolled infection resulting from human immunodeficiency virus (HIV) and/or active hepatitis

• 9. Reported history of drug or alcohol abuse within the past 12 months

• 10. History of hypersensitivity reaction to inhaled anticholinergics, sympathomimetic amines, or inhaled medication or any component thereof (including report of paradoxical bronchospasm)

• 11. History of acute urinary retention, treatment refractory benign prostatic hyperplasia (BPH), bladder neck obstruction, or narrow-angle glaucoma (Note: Patients with controlled, stable BPH are not excluded)

• 12. Patients unable to use a multidose DPI or a pressurized metered-dose inhaler

• 13. Treatment with any other investigational drug within 30 days (or 6 half-lives, whichever is longer) before Visit 1A

• 14. Women who are pregnant or breastfeeding

• 15. Use of any prohibited medication listed in Appendix II

• 16. Employee or immediate relative of an employee of AstraZeneca, any of its affiliates or partners, or the study center

Related Conditions & MeSH terms

• Chronic Obstructive Pulmonary Disease
• COPD
• Lung Diseases
• Lung Diseases, Obstructive
• Moderate to Very Severe COPD
• Pulmonary Disease, Chronic Obstructive

Intervention

Drug:
• Aclidinium Bromide
400 µg, twice per day, oral administration via a multi-dose dry-powder inhaler (DPI)
• Placebo
Dose matched placebo, twice per day, oral administration via a multi-dose dry-powder inhaler (DPI)

Locations

Country	Name	City	State
Canada	Research Site	Ajax	Ontario
Canada	Research Site	Bridgewater	Nova Scotia
Canada	Research Site	Burlington	Ontario
Canada	Research Site	Cornwall	Ontario
Canada	Research Site	Dorchester	Ontario
Canada	Research Site	Edmonton	Alberta
Canada	Research Site	Edmonton	Alberta
Canada	Research Site	Halifax	Nova Scotia
Canada	Research Site	Hamilton	Ontario
Canada	Research Site	Kamloops	British Columbia
Canada	Research Site	Kelowna	British Columbia
Canada	Research Site	Langley	British Columbia
Canada	Research Site	London	Ontario
Canada	Research Site	London	Ontario
Canada	Research Site	Longueuil	Quebec
Canada	Research Site	Montreal	Quebec
Canada	Research Site	Newmarket	Ontario
Canada	Research Site	Penticton	British Columbia
Canada	Research Site	Quebec
Canada	Research Site	Quebec
Canada	Research Site	Saskatoon	Saskatchewan
Canada	Research Site	St Charles Borromee	Quebec
Canada	Research Site	St. John's	Newfoundland and Labrador
Canada	Research Site	Sudbury	Ontario
Canada	Research Site	Sudbury	Ontario
Canada	Research Site	Thorold	Ontario
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Canada	Research Site	Toronto	Ontario
Canada	Research Site	Toronto	Ontario
Canada	Research Site	Toronto	Ontario
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Canada	Research Site	Windsor	Ontario
Canada	Research Site	Winnipeg	Manitoba
United States	Research Site	Abingdon	Virginia
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United States	Research Site	Altoona	Pennsylvania
United States	Research Site	Amarillo	Texas
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United States	Research Site	Tabor City	North Carolina
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United States	Research Site	Tampa	Florida
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United States	Research Site	Towson	Maryland
United States	Research Site	Troy	Michigan
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United States	Research Site	Tucson	Arizona
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United States	Research Site	Tullahoma	Tennessee
United States	Research Site	Tulsa	Oklahoma
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United States	Research Site	Tuscaloosa	Alabama
United States	Research Site	Tyler	Texas
United States	Research Site	Union	South Carolina
United States	Research Site	Uniontown	Pennsylvania
United States	Research Site	Valparaiso	Indiana
United States	Research Site	Vero Beach	Florida
United States	Research Site	Vista	California
United States	Research Site	Waco	Texas
United States	Research Site	Wappingers Falls	New York
United States	Research Site	Waterbury	Connecticut
United States	Research Site	Webster	Texas
United States	Research Site	Westfield	New York
United States	Research Site	Westminster	California
United States	Research Site	Wheat Ridge	Colorado
United States	Research Site	Whiteville	North Carolina
United States	Research Site	Wildomar	California
United States	Research Site	Wilmington	Delaware
United States	Research Site	Wilmington	North Carolina
United States	Research Site	Winston-Salem	North Carolina
United States	Research Site	Winston-Salem	North Carolina
United States	Research Site	Winter Park	Florida
United States	Research Site	Woodstock	Georgia
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United States	Research Site	Yukon	Oklahoma
United States	Research Site	Zachary	Louisiana

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of Moderate or Severe Chronic Obstructive Pulmonary Disease (COPD) Exacerbations Per Subject Per Year During the First Year of Treatment	The rate (number of events per subject per year) of moderate or severe COPD exacerbations during the first year of treatment based on on-treatment analysis with treatment group, baseline inhaled corticosteroids (ICS) use, baseline COPD severity, history of at least 1 exacerbation in the past year, and smoking status as factors and the log of the exposure time adjusted for the time the subjects experienced exacerbations as an offset variable.	12 months
Primary	Number of Participants With Major Adverse Cardiovascular Event (MACE) - on Study Analysis	To assess the cardiovascular (CV) safety of aclidinium bromide on MACEs. The number of subjects with an adjudicated composite MACE with treatment group, baseline CV severity, and smoking status as factors. MACE for the analyses was defined as any adjudicated event which was a composite of the total of CV death, non-fatal myocardial infarction (MI), or non-fatal stroke (on-study analysis).	At Screening, Treatment period (upto 36 months) and Post-treatment follow-up (PTFU)
Secondary	Rate of Hospitalizations Due to COPD Exacerbation Per Subject Per Year During the First Year of Treatment- on Treatment Analysis	To assess whether aclidinium bromide reduces moderate or severe COPD exacerbations. The rate of hospitalization (number of events per subject per year) due to COPD exacerbations during the first year of treatment based on on-treatment analysis with treatment group, baseline ICS use, baseline COPD severity, history of at least 1 exacerbation in the past year, and smoking status as factors and the log of the exposure time adjusted for the time the subjects experienced exacerbations as an offset variable.	12 months
Secondary	Number of Participants With Major Adverse Cardiovascular Event (MACE) or Other Serious Cardiovascular Events of Interest - On-study Analysis	To assess the CV safety of aclidinium bromide on MACEs. The number of subjects with an adjudicated MACE or other serious CV events of interest with treatment group, baseline CV severity, and smoking status as factors.; Other serious CV events included events from Cardiac tachyarrhythmias plus preferred terms (PTs) Tachycardia, Heart rate increase, and Palpitation; Cardiac failure; Bradycardia and PTs Sinus arrest and Sinus bradycardia; Conduction defects; Conditions associated with Central nervous system haemorrhages and cerebrovascular accidents; and selected PTs included in the Other ischemic heart disease.	At Screening, Treatment period (upto 36 months) and Post-treatment follow-up (PTFU)

External Links

•   Protocol
•   Statistical Analysis Plan (SAP)