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Sanofi, Regeneron Trial Meets Primary Endpoint

Showing Praluent® Injection significantly reduced the risk of major adverse cardiovascular events

Sanofi and Regeneron Pharmaceuticals announced that the ODYSSEY OUTCOMES trial met its primary endpoint, showing Praluent® (alirocumab) Injection significantly reduced the risk of major adverse cardiovascular events (MACE) in patients who had suffered a recent acute coronary syndrome (ACS) event such as a heart attack.    Key findings include:   On the primary endpoint, Praluent reduced the overall risk of MACE by 15% (HR=0.85, CI: 0.78-0.93, p=0.0003). The MACE composite end...

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