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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)

2015;16(suppl 1):7790

Approval for treatment is not guaranteed

vomiting 2%6% vs

Patients may continue seeing their primary care physician while also engaging with a telehealth provider