A Phase 3 multi-centre study to test the efficacy, safety and tolerability of Bococizumab (PF-04950615) administered subcutaneously in reducing the occurrence ofmajor cardiovascular events due to clogging up of arteries by fatty substances in high risk subjects.
- Conditions
- artherosclerosisMedDRA version: 20.0Level: LLTClassification code 10003601Term: AtherosclerosisSystem Organ Class: 100000022953Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
- Registration Number
- EUCTR2013-002795-41-DE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 11000
1. Informed Consent
There must be evidence of personally signed and dated informed consent documents for both the pre-screening and screening visits, indicating that the subject (or a legal representative) has been informed of all pertinent aspects of the study. The pre-screening visit informed consent form will be limited to study activities up until the screening visit. The screening visit informed consent form will cover all aspects of the study. Subjects should be reconsented if there are modifications to the original
informed consent document, at the next available opportunity.
2. Compliance
Subjects must be willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
3. Age
For subjects who have had a prior CVD event, or who have a condition of elevated LDL-C without a prior CVD event (heterozygous familial hypercholesterolemia [heFH] or an LDL-C=190 mg/dL [4.9 mmol/L]), subjects must be men or women age= the legal age of majority (legal adulthood), in the subject’s country. For other subjects who have not had a prior CVD event, men must be age =50 years and women must be age=60 years.
4. Acceptance of administration of IP Subjects must be willing and able to self-administer or be administered sub-cutaneous injections of IP.
5. Requirements for background lipid lowering treatment
There should be no plans at the time of pre-screening and randomization to modify the dose of statin for the duration of the trial. Unless the background lipid lowering treatment exceptions described below are met, subjects must be treated with one of the following highly effective statins at the specified daily doses for =4 weeks prior to the pre-screening visit:
-atorvastatin, 40 milligrams (mg) once a day;
- rosuvastatin, 20 mg, once a day;
- simvastatin 40 mg, once a day or, if a subject has been on that dose for >1 year, 80 mg, once a day.
Combination medications that contain atorvastatin, rosuvastatin, or simvastatin components described at the aforementioned doses will be permitted. Background lipid lowering treatment exceptions
The following background lipid lowering treatment exceptions are permitted:
-Lower doses of statins due to partial statin intolerance
Subjects may be on a lower dose of one of the highly effective statins described above if there is documented intolerance to any one of them (atorvastatin, rosuvastatin, or simvastatin) at the aforementioned, or lower, doses. Intolerance to any dose of any statin must be documented as historical adverse events attributed to the statin in question, in the source documentation and case report form (CRF).
- Regulatory limitations
Subjects may be on a lower dose of one of the highly effective statins described above if the highest locally approved dose for one of the stated statins is lower than those doses shown above (eg, in Japan, atorvastatin 20 mg, once a day, is the highest locally approved dose) or due to label restrictions.
- Alternative statins
Subjects may be treated with other statins (pravastatin, fluvastatin, pitavastatin, or lovastatin), different from the highly effective statins listed above, if there is documented intolerance to any two different highly effective statins (atorvastatin, rosuvastatin, simvastatin) at the lowest available daily dose for at least one of those highly effective statins. Intolerance to any statin must be documented as historical adverse events attributed to the statin in question,
1. Personnel involved in the conduct of the study
Subjects who are investigational site staff members directly involved in the conduct of the trial and their family members, site staff members otherwise supervised by the Investigator, or subjects who are Pfizer employees directly involved in the conduct of the trial.
2. Exclusionary prior CV events or planned revascularization procedures
-A planned coronary (PCI or CABG) or other arterial revascularization;
-Myocardial infarction, stroke, or any non-coronary arterial revascularization= 30 days prior to screening;
-Coronary revascularization= 90 days prior to screening.
3. Participation in prior clinical research studies
Participation in other studies involving small molecule investigational drug(s) (Phases 1-4) within 1 month, or five half-lives, of Visit 1, whichever is longer; any
participation in a cholesteryl ester transfer protein (CETP) inhibitor within 1 year of Visit 1; or any biological agents within 6 months or 5 half-lives, of Visit 1, whichever is longer (the investigator should refer to documents provided by the subject on the other study to determine the IP half-life). If the blind of the prior study has been broken and the investigator provides documentation that the subject received placebo, the potential subject can be included, regardless of when participation occurred.
4. Other exclusionary conditions
Other severe, acute, or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or IP administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.
5. Childbearing potential and/or breast feeding
Pregnant females; breastfeeding females; males and females of childbearing potential who are unwilling or unable to use a highly effective method of contraception as outlined in this protocol for the duration of the study and for 63 days after last dose of investigational product
6. Latex sensitivity
Latex sensitive individuals (due to potential for exposure to natural dry rubber in the prefilled syringe cap of investigational product, during administration).
7. Apheresis
Undergoing lipid apheresis, within 6 weeks of pre-screening, or planned start of lipid apheresis.
8. Severe congestive heart failure
Congestive heart failure of New York Heart Association (NYHA) Class IV, or if there is prior documentation of left ventricular ejection fraction (LVEF) of <25%, measured by imaging.
9. Dialysis
Potential subjects with end stage renal disease on dialysis.
10. Chronic renal insufficiency
Potential subjects with an eGFR of <30 ml/min/1.73m2 by MDRD formula at Visit 1.
11. Hypertension
Poorly controlled hypertension at any screening visit or at randomization, defined as the average of two systolic blood pressure (BP) measurements >180 mmHg or the average of two diastolic BP measurements >110 mmHg even with treatment. Subjects who have hypertension and are controlled on stable doses of anti-hypertensive medications may be included. An additional set of BP measurements may be performed within the hour or at the completion of the office visit, to determine if a subject may be included in the study, given the potential for white coat hypertension.” The final set of measurements will be the measurements of record.
12. Cerebral hemorrhage risk
A prior history of hemorrhag
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method