drugset / Trial / NCT01975389

The Evaluation of Bococizumab (PF-04950615; RN316) in Reducing the Occurrence of Major Cardiovascular Events in High Risk Subjects

NCT01975389 ↗

Phase 3 Terminated 10564 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study evaluates the PCSK9 inhibitor, Bococizumab (PF-04950615;RN316), compared to placebo, in reducing the occurrrence of major cardiovascular events, including cardiovascular death, myocardial infarction, stroke, and unstable angina requiring urgent revascularization in high risk subjects who are receiving background lipid lowering therapy and have cholesterol laboratory values of LDL-C \>/= 100 mg/dL (2.6 mmol/L) or non-HDL-C \>/=130 mg/dL (3.4 mmol/L).

Timeline

Start
2013-10-29
Primary completion
2017-04-03
Completion
2017-04-03

Outcome

Met primary endpoint

Stopped: “See Detailed Description”

registry analysis (superiority test); Placebo vs Bococizumab (PF-04950615); p = 0.021469; Hazard Ratio (HR) 0.79 (95% CI 0.65 to 0.97); Log Rank NCT01975389 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bococizumab Monoclonal antibody 150 mg Subcutaneous