E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
chronic Coronary Heart Disease (cCHD) |
|
MedDRA Classification |
E.1.3 | Condition being studied is a rare disease | No |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
The primary objective of this study is to evaluate clinical efficacy of long-term treatment with darapladib Enteric Coated tablets, 160 mg (oral once daily dose) as compared to placebo when added to standard of care in a chronic Coronary Heart Disease (CHD) patient population on the incidence of first occurrence of the composite of Major Adverse Cardiovascular Events (MACE) (cardiovascular death, non-fatal Myocardial Infarction (MI), non-fatal stroke). |
|
E.2.2 | Secondary objectives of the trial |
The secondary objectives are to evaluate the efficacy of darapladib on major and total coronary events (including CHD death, non-fatal MI, urgent and non-urgent coronary revascularization, or hospitalization for unstable angina), individual components of MACE and all-cause mortality. Additional safety and efficacy parameters including relations to and changes of biomarkers of CV risk, health economic outcomes, and adverse events (AEs) will also be evaluated. |
|
E.2.3 | Trial contains a sub-study | Yes |
E.2.3.1 | Full title, date and version of each sub-study and their related objectives |
There are several sub-studies (appendixes 8 -11 of protocol, same date and version as main protocol): - A substudy on the investigation of the effect of darapladib on rate of progression of albuminuria as assessed by change in urine Albumin:Creatinine Ratio (ACR) in subjects with diabetes mellitus. - A substudy on the effect of darapladib on systolic blood pressure as assessed by 24-hour ambulatory blood pressure monitoring. - A substudy on the effect of darapladib on rate of decline in cognitive function. - Population Pharmacokinetic and Pharmacokinetic/Pharmacodynamic Substudies.
|
|
E.3 | Principal inclusion criteria |
1. Signed written informed consent prior to beginning study-related procedures (subject must understand the aims, investigational procedures and possible consequences of the study). 2. Male or female aged at least 18 years, inclusive, at screening. Female subjects must be post-menopausal or using a highly effective method for avoidance of pregnancy. The decision to include or exclude women of childbearing potential may be made at the discretion of the investigator in accordance with local practice in relation to adequate contraception. 3. Current treatment with statin therapy unless not indicated according to treatment guidelines or contraindicated in the opinion of the investigator. 4. Chronic CHD documented by at least one of the following: a.prior MI (>1 month prior to randomization). b. prior coronary revascularization procedure [percutaneous coronary intervention (PCI) > 1 month prior to randomization or coronary artery bypass graft (CABG) >3 months prior to randomization]. c. multivessel CHD involving major epicardial coronary arteries confirmed by coronary angiography at any time (without revascularization). AND 5. At least one of the following additional predictors of CV risk [a through f]: a. age >60 years at randomization. b. diabetes mellitus requiring pharmacotherapy. c. HDL-C <40 mg/dL (1.03 mmol/L). d. smoker (defined as at least 5 cigarettes per day on average) or a previous smoker (defined as at least 5 cigarettes per day on average when smoking) who discontinued within the past 3 months. e. significant renal dysfunction (defined as estimated glomerular filtration rate [eGFR] ≥30 and </=59 mL/min per 1.73 m2 OR urine ACR ≥30 mg albumin/g creatinine). f. polyvascular disease manifested as coexistent clinically diagnosed arterial disease in at least 2 arterial territories, defined as: • chronic CHD and cerebrovascular disease defined as carotid artery disease or prior ischemic stroke >3 months. OR • chronic CHD and peripheral arterial disease (PAD).
|
|
E.4 | Principal exclusion criteria |
1. Planned coronary revascularization (PCI or CABG) or any other major surgical procedure. 2. Current liver disease, known hepatic or biliary abnormalities (with the exception of Gilbert’s syndrome or asymptomatic gallstones) or evidence of abnormal liver function tests [total bilirubin or alkaline phosphatase >1.5 x upper limit of normal (ULN); or ALT or AST >2.5 x ULN] or other hepatic abnormalities that in the opinion of the Investigator would preclude the subject from participation in the study. 3. Severe renal impairment (eGFR <30 mL/min/1.73 m2) or history of nephrectomy or kidney transplant (regardless of renal function). 4. Current severe heart failure (New York Heart Association class III or IV). 5. Poorly controlled hypertension despite lifestyle modifications and pharmacotherapy. 6. Any life-threatening condition with life expectancy <2 years, other than vascular disease, that might prevent the subject from completing the study (e.g., very severe chronic airways disease, known human immunodeficiency virus [HIV] positive, or cancer in the past five years other than non-melanoma skin cancer). 7. Severe asthma that is poorly controlled on pharmacotherapy. 8. Positive pregnancy test (all female subjects of childbearing potential must have a urine B-human chorionic gonadotropin [hCG] pregnancy test performed at Screening and/or within 7 days prior to randomization) or is known to be pregnant or lactating. 9. History of anaphylaxis, anaphylactoid (resembling anaphylaxis) reactions, or severe allergic responses. 10. Alcohol or drug abuse within the past 6 months, or current mental condition (psychiatric disorder, senility or dementia), which may affect study compliance or prevent understanding of the aims, investigational procedures or possible consequences of the study. 11. Current or planned chronic administration of strong oral or injectable cytochrome P-450 isoenzyme 3A4 (CYP3A4) inhibitors. 12. Subjects with both parents of Japanese, Chinese, or Korean ancestry must have a blood sample collected for assessment of Lp-PLA2 activity by the central laboratory prior to randomization. Those with Lp-PLA2 activity </=20.0 nmol/min/mL will be excluded from participation in the study.13. Previous exposure to darapladib (SB-480848). 14. Use of another investigational product within 30 days or 5 half-lives (whichever is the longer) preceding the first dose of darapladib or matching placebo. 15. Currently in a study of an investigational device. 16. Any other reason the investigator deems the subject to be unsuitable for the study.
|
|
E.5 End points |
E.5.1 | Primary end point(s) |
The primary efficacy endpoint is the time to the first occurrence of any component of the composite of major adverse cardiovascular events (MACE: CV death, non-fatal MI, or non-fatal stroke) in a chronic CHD population treated with darapladib enteric coated tablets, 160 mg compared with placebo.
|
|
E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | Yes |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | Yes |
E.6.7 | Pharmacodynamic | Yes |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | Yes |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | Yes |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | No |
E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 4 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 265 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
|
E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
|
The trial should end with the last subject's in-clinic follow-up visit . |
|
E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 3 |
E.8.9.1 | In the Member State concerned months | 10 |
E.8.9.1 | In the Member State concerned days | 0 |
E.8.9.2 | In all countries concerned by the trial years | 3 |
E.8.9.2 | In all countries concerned by the trial months | 10 |
E.8.9.2 | In all countries concerned by the trial days | 0 |