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Ro connected its platform with Eli Lilly's direct-to-patient offering in December 2024 to expand access to FDA-approved, authentic Zepbound

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Disclaimer: This guide is for research and educational purposes only

All patients should see a doctor for guidance on proper use

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ELIXA trial included patients with recent cardiovascular event (patients with acute coronary syndrome 180 days before randomization), and although there was no benefit in MACE reduction in lixisenatide treated patients compared to placebo, results revealed cardiovascular safety of lixisenatide in this specific high risk population (38, 40)