A Study to Assess the Efficacy and Safety of Enteric-Coated Acetylsalicylic Acid in Patients at Moderate Risk of Cardiovascular Disease (ARRIVE)
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Purpose
The use of acetylsalicylic acid in the primary prevention of cardiovascular events has been extensively studied. However, the overall risk level of the study populations was low (< 10% 10-year CHD risk). The current study is designed to prove the efficacy and tolerability of 100 mg enteric-coated Aspirin versus placebo in the prevention of cardiovascular disease (CVD) events, which include fatal and nonfatal myocardial infarction, fatal and nonfatal stroke and CV death, in a population with no history of known CVD who are at moderate risk of major CHD events (approximately 10-20% 10 year CHD risk). This corresponds to a patient population mean 10-year CVD risk of approximately 30%. Subjects are treated in a standard care setting and may receive treatment for the underlying risk factors as defined by the treating physician. Outcome events will be adjudicated by an Endpoint Adjudication Committee and the study will be monitored by an independent Data Safety Monitoring Board.
| Condition | Intervention | Phase |
|---|---|---|
|
Moderate Risk of CVD |
Drug: Aspirin (Acetylsalicylic acid, BAYE4465) Drug: Placebo |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | A Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel Group Study to Assess the Efficacy (Reduction of Cardiovascular Disease Events) and Safety of 100 mg Enteric-Coated Acetylsalicylic Acid in Patients at Moderate Risk of Cardiovascular Disease |
- Time to first occurrence of the composite outcome of MI, stroke or cardiovascular death [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Time to first occurrence of the composite outcome of cardiovascular death, ACS (Acute Coronary Syndrome), or stroke [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Time to first occurrence of the individual components of the primary: non-fatal MI, total MI, non-fatal stroke, total stroke or cardiovascular death [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Time to incidence of all cause mortality [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Time to first occurrence of/ incidence of all cancers, excluding non melanoma skin cancer [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Time to first occurrence of/ incidence of colon cancer [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Incidence of MI, stroke and CV death separately [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: No ]
- Incidence of treatment-emergent adverse events (observed and reported), and changes in the physical examination findings, weight, and vital signs [ Time Frame: Approximately 5 years of follow-up (duration of planned treatment phase) ] [ Designated as safety issue: Yes ]
| Enrollment: | 12590 |
| Study Start Date: | July 2007 |
| Estimated Study Completion Date: | May 2015 |
| Estimated Primary Completion Date: | May 2015 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Arm 1 |
Drug: Aspirin (Acetylsalicylic acid, BAYE4465)
100mg enteric coated Aspirin, taken daily
|
| Placebo Comparator: Arm 2 |
Drug: Placebo
Placebo, taken daily
|
Eligibility| Ages Eligible for Study: | 55 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Males aged 55 years and above with 2 to 4 risk factors. Male Risk Factors:
- Elevated cholesterol (Tchol>200 mg/dL or LDL>130 mg/dL; as measured at screening) irrespective of current treatment
- Current smoking: defined as any cigarette smoking in the past 12 months
- Low HDL cholesterol (HDL<40 mg/dL; as measured at screening)
- Elevated blood pressure (SBP>140 mmHg; as measured at screening)
- Currently on any medication to treat high blood pressure
- Positive family history of early CHD (a first-degree relative [father, mother, brother, sister, son, daughter] suffered a heart attack [myocardial infarction] before the age of 60 years)
Females aged 60 and above with 3 or more risk factors. Female Risk Factors:
- Elevated cholesterol (Tchol>240 mg/dL or LDL>160 mg/dL; as measured at screening) irrespective of current treatment
- Current smoking: defined as any cigarette smoking in the past 12 months
- Low HDL cholesterol (HDL<40 mg/dL; as measured at screening)
- Elevated blood pressure (SBP>140 mmHg; as measured at screening)
- Currently on any medication to treat high blood pressure
- Positive family history of early CHD (a first-degree relative [father, mother, brother, sister, son, daughter] suffered a heart attack [myocardial infarction] before the age of 60 years)
- An understanding and willingness to comply with trial procedures and has given written informed consent to participate in the trial
Exclusion Criteria:
- History of a documented vascular event, such as MI, stroke, coronary artery angioplasty or stenting, coronary artery bypass graft, relevant arrhythmias, or congestive heart failure or vascular intervention
- Patients who are at higher than moderate risk on the basis of their diabetes status, other factors known to the investigator, or the currently used national risk score
- Known contraindications to the study drug, e.g. hypersensitivity to acetylsalicylic acid
- Recent (in the past year) history of gastrointestinal or genitourinary bleeding or other bleeding disorders
- Active diagnosed and documented reflux esophagitis
- Patients presenting with any medical condition, or psychiatric or substance abuse disorder, that, in the opinion of the investigator, is likely to affect the patient's ability to complete the study or precludes the patient's participation in the study
- Lactating women or women of childbearing potential
- Severe liver disease or damage based on the clinical judgment of the investigator
- Severe renal disease or damage based on the clinical judgement of the investigator
- A definite indication for acetylsalicylic acid therapy, other antiplatelet drug, or anticoagulant in the opinion of the physician
- A history of asthma induced by administration of salicylates or substances with a similar action, notably NSAIDS
- Chronic, frequent (> 5 days/month) use of NSAIDs (including aspirin, or aspirin containing products), COX-2 inhibitors or metamizole
- Current participation in any other trials involving investigational products within 30 days prior to the Screening Visit
- Current use of an anticoagulant medication
- Sitting systolic blood pressure greater than 170 mmHg
Contacts and Locations
Show 669 Study Locations| Study Director: | Bayer Study Director | Bayer |
More Information
Additional Information:
No publications provided by Bayer
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Head Medical Affairs, Bayer HealthCare LLC, Consumer Care |
| ClinicalTrials.gov Identifier: | NCT00501059 History of Changes |
| Other Study ID Numbers: | 12198, 2006-003622-29 |
| Study First Received: | July 12, 2007 |
| Last Updated: | March 25, 2013 |
| Health Authority: | United States: Food and Drug Administration Germany: Federal Institute for Drugs and Medical Devices Ireland: Irish Medicines Board Italy: Ethics Committee Poland: Ministry of Health Spain: Agencia Española de Medicamentos y Productos Sanitarios United Kingdom: Medicines and Healthcare Products Regulatory Agency |
Keywords provided by Bayer:
|
Primary prevention of coronary heart disease Stroke and cardiovascular death Aspirin |
Additional relevant MeSH terms:
|
Cardiovascular Diseases Aspirin Anti-Inflammatory Agents, Non-Steroidal Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Anti-Inflammatory Agents Therapeutic Uses |
Antirheumatic Agents Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Cardiovascular Agents Hematologic Agents Platelet Aggregation Inhibitors Cyclooxygenase Inhibitors Enzyme Inhibitors Antipyretics Central Nervous System Agents |
ClinicalTrials.gov processed this record on June 18, 2013