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The subgroup analyses of each article found the following results in relation to the risk of stroke: In the ELIXA lixisenatide trial that evaluated patients with acute coronary syndrome (n = 6068 patients with an acute coronary event within 180 days before screening), subcutaneous (sc.) lixisenatide had no effect on the risk of nonfatal stroke over a median 25-month follow-up [16]
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