drugset / Trial / NCT01968980

A 52 Week Study To Assess The Use Of Bococizumab (PF-04950615; RN316) In Subjects With Heterozygous Familial Hypercholesterolemia

NCT01968980 ↗

Phase 3 Completed 370 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, randomized study in subjects with heterozygous familial hypercholesterolemia receiving highly effective statins to assess the safety, efficacy and tolerability of Bococizumab (PF-04950615; RN316) to lower LDL-C.

Timeline

Start
2013-10-23
Primary completion
2016-04-15
Completion
2016-04-15

Outcome

Met primary endpoint

registry Placebo vs PF--04950615; p <0.001; Least square (LS) mean difference -54.5 (95% CI -59.5 to -49.5) NCT01968980 ↗

release “Pfizer Inc. announced two additional Phase 3 bococizumab trials, SPIRE-HR ( H igh R isk) and SPIRE-FH ( F amilial H ypercholesterolemia), met their primary endpoint” pfizer.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bococizumab Monoclonal antibody 150 mg Subcutaneous