Amgen IncPhase 3 trial shows Repatha cuts death risk by 20%, a significant efficacy result.

Amgen announced that a pre-specified analysis of its Phase 3 VESALIUS-CV trial showed Repatha (evolocumab) reduced the risk of death by 20% in high-risk adults without a prior heart attack or stroke when added to statins or other LDL-C-lowering treatments. The analysis demonstrated meaningful reductions in both overall and cardiovascular deaths, with the mortality benefit emerging after about 1.5 years of treatment and continuing through a median follow-up of 4.6 years. Repatha also reduced heart attack risk within six months of treatment initiation in a separate analysis. The findings were presented at the European Society of Cardiology Congress 2026 in Munich and published simultaneously in Circulation. Repatha, a human monoclonal antibody targeting PCSK9, was first approved in 2015 and has been used by approximately 9 million patients globally; in August 2025, the U.S. Food and Drug Administration broadened its approved use to include adults at increased risk for major adverse cardiovascular events due to uncontrolled LDL-C.
Amgen IncPhase 3 trial shows Repatha cuts death risk by 20%, a significant efficacy result.