How could the positive VESALIUS-CV trial results affect Mass General Brigham's standing?
Mass General Brigham benefits from positive Amgen trial results The announcement of the VESALIUS-CV trial results, which showed Amgen's Repatha drug was cost-effective and significantly reduced cardiovascular risk, enhances the clinical reputation of Mass General Brigham. The trial was led by the Duke Clinical Research Institute in collaboration with the TIMI Study Group, which included Mass General Brigham. The results showed Repatha cut the combined risk of coronary heart disease death, heart attack, or ischemic stroke by 25% over a median of about 4.6 years. Furthermore, the health economic analysis found the drug was cost-effective for high-risk adults, coming in about 36% below the $120,000 per QALY benchmark set by the AHA and ACC.
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Amgen announced results from the VESALIUS-CV trial, presenting a health economic analysis of its cholesterol drug Repatha. The analysis found Repatha to be cost-effective for high-risk adults who have never had a heart attack or stroke. This cost was approximately 36% below a benchmark used by the American College of Cardiology and American Heart Association. The analysis was led by the Duke Clinical Research Institute in collaboration with Mass General Brigham and Harvard.
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The VESALIUS-CV trial, which Mass General Brigham was part of through the TIMI Study Group, yielded positive results. These results showed that Repatha cut the combined risk of coronary heart disease death, heart attack, or ischemic stroke by 25% over a median of about 4.6 years. This successful outcome, combined with the finding that the drug is cost-effective, validates the clinical research and expertise of the participating institutions.
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- medicaldaily.com Tuesday
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The facts so far
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- The trial was led by the Duke Clinical Research Institute in collaboration with the TIMI Study Group at Mass General Brigham and Harvard.medicaldaily.com
- Repatha cut the combined risk of coronary heart disease death, heart attack or ischemic stroke by 25% over a median of about 4.6 years.medicaldaily.com
- The drug was found to be about 36% below a benchmark used by the American College of Cardiology and American Heart Association.medicaldaily.com
- The 2025 AHA and ACC cost and value statement sets $120,000 per QALY as that threshold.medicaldaily.com
Why it matters
For Mass General Brigham, participation in high-profile, successful clinical trials like VESALIUS-CV reinforces its standing as a leader in cardiovascular research. Positive results, especially those demonstrating both clinical efficacy and cost-effectiveness, are crucial for attracting top medical talent, securing research funding, and maintaining its reputation among patients and peers.
This outcome is part of a broader trend where major academic medical centers collaborate with pharmaceutical companies and research institutes to drive medical innovation. The collaboration between Duke, Harvard, and Mass General Brigham highlights the power of large-scale, multi-institutional studies in establishing new standards of care and demonstrating the value of new treatments.
What we don't know yet
- Will the full analysis of the VESALIUS-CV trial appear in a peer-reviewed journal?
- How will the cost-effectiveness finding influence insurance coverage rules for Repatha?
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Reporting
- medicaldaily.comTuesday
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